This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA1107947869
Gene: BRAF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140787309_140787324dup , CM000669.2:g.140787309_140787324dup GRCh38
NC_000007.13:g.140487109_140487124dup , CM000669.1:g.140487109_140487124dup GRCh37
NC_000007.12:g.140133578_140133593dup NCBI36
NG_007873.3:g.142449_142464dup , LRG_299:g.142449_142464dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1177+232_1177+247dup MANE Select ENSP00000493543.1:n.1177+232_1177+247dup
ENST00000288602.11:c.1177+232_1177+247dup ENSP00000288602.7:n.1177+232_1177+247dup
ENST00000496384.7:c.1177+232_1177+247dup ENSP00000419060.2:n.1177+232_1177+247dup
ENST00000497784.2:c.*627+232_*627+247dup ENSP00000420119.2:n.*627+232_*627+247dup
ENST00000642228.1:c.*255+232_*255+247dup ENSP00000493678.1:n.*255+232_*255+247dup
ENST00000642875.1:n.619+232_619+247dup
ENST00000644120.1:n.1567+232_1567+247dup
ENST00000644650.1:c.273+232_273+247dup
ENST00000644905.1:n.1266+232_1266+247dup
ENST00000644969.2:c.1177+232_1177+247dup MANE Plus Clinical ENSP00000496776.1:n.1177+232_1177+247dup
ENST00000646730.1:c.1177+232_1177+247dup ENSP00000494784.1:n.1177+232_1177+247dup
ENST00000646891.1:c.1177+232_1177+247dup ENSP00000493543.1:n.1177+232_1177+247dup
ENST00000647434.1:c.220+232_220+247dup ENSP00000495132.1:n.220+232_220+247dup
ENST00000288602.10:c.1177+232_1177+247dup ENSP00000288602.6:n.1177+232_1177+247dup
ENST00000497784.1:c.1212+232_1212+247dup ENSP00000420119.1:n.1212+232_1212+247dup
NM_004333.4:c.1177+232_1177+247dup , LRG_299t1:c.1177+232_1177+247dup NP_004324.2:n.1177+232_1177+247dup
XM_005250045.1:c.1177+232_1177+247dup XP_005250102.1:n.1177+232_1177+247dup
XM_005250046.1:c.1177+232_1177+247dup XP_005250103.1:n.1177+232_1177+247dup
XM_011516529.1:c.1177+232_1177+247dup XP_011514831.1:n.1177+232_1177+247dup
XM_011516530.1:c.1177+232_1177+247dup XP_011514832.1:n.1177+232_1177+247dup
XR_242190.1:n.1185+232_1185+247dup
XR_927520.1:n.1185+232_1185+247dup
XR_927521.1:n.1185+232_1185+247dup
XR_927522.1:n.1185+232_1185+247dup
XR_927523.1:n.1185+232_1185+247dup
NM_001354609.1:c.1177+232_1177+247dup NP_001341538.1:n.1177+232_1177+247dup
NM_004333.5:c.1177+232_1177+247dup NP_004324.2:n.1177+232_1177+247dup
NR_148928.1:n.1482+232_1482+247dup
XM_017012558.1:c.1177+232_1177+247dup XP_016868047.1:n.1177+232_1177+247dup
XM_017012559.1:c.1177+232_1177+247dup XP_016868048.1:n.1177+232_1177+247dup
XR_001744857.1:n.1185+232_1185+247dup
XR_001744858.1:n.1185+232_1185+247dup
NM_001354609.2:c.1177+232_1177+247dup NP_001341538.1:n.1177+232_1177+247dup
NM_001374244.1:c.1177+232_1177+247dup NP_001361173.1:n.1177+232_1177+247dup
NM_001374258.1:c.1177+232_1177+247dup MANE Plus Clinical NP_001361187.1:n.1177+232_1177+247dup
NM_004333.6:c.1177+232_1177+247dup MANE Select NP_004324.2:n.1177+232_1177+247dup
NM_001378467.1:c.1186+232_1186+247dup NP_001365396.1:n.1186+232_1186+247dup
NM_001378468.1:c.1177+232_1177+247dup NP_001365397.1:n.1177+232_1177+247dup
NM_001378469.1:c.1177+232_1177+247dup NP_001365398.1:n.1177+232_1177+247dup
NM_001378470.1:c.1075+232_1075+247dup NP_001365399.1:n.1075+232_1075+247dup
NM_001378471.1:c.1141-4233_1141-4218dup NP_001365400.1:n.1141-4233_1141-4218dup
NM_001378472.1:c.1021+232_1021+247dup NP_001365401.1:n.1021+232_1021+247dup
NM_001378473.1:c.1021+232_1021+247dup NP_001365402.1:n.1021+232_1021+247dup
NM_001378474.1:c.1177+232_1177+247dup NP_001365403.1:n.1177+232_1177+247dup
NM_001378475.1:c.913+232_913+247dup NP_001365404.1:n.913+232_913+247dup
Search 100 bp 5'
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