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: CA3091079264
Community Standard Title: NM_005633.4(SOS1):c.720+69A=
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054545T= , CM000664.2:g.39054545T= GRCh38
NC_000002.11:g.39281686T= , CM000664.1:g.39281686T= GRCh37
NC_000002.10:g.39135190T= NCBI36
NG_007530.1:g.70919A= , LRG_754:g.70919A=

Transcript Alleles

HGVS Amino-acid Change
NM_005633.4:c.720+69A= MANE Select NP_005624.2:n.720+69A=
ENST00000402219.8:c.720+69A= MANE Select ENSP00000384675.2:n.720+69A=
NM_001382394.1:c.699+69A= NP_001369323.1:n.699+69A=
NM_001382395.1:c.720+69A= NP_001369324.1:n.720+69A=
NM_005633.3:c.720+69A= , LRG_754t1:c.720+69A= NP_005624.2:n.720+69A=
ENST00000395038.6:c.720+69A= ENSP00000378479.2:n.720+69A=
ENST00000402219.6:c.720+69A= ENSP00000384675.2:n.720+69A=
ENST00000426016.5:c.720+69A= ENSP00000387784.1:n.720+69A=
ENST00000461545.2:n.747+69A=
ENST00000685782.1:n.1558+69A=
ENST00000688189.1:n.554A=
ENST00000689668.1:n.727+69A=
ENST00000690679.1:c.820+69A=
ENST00000690876.1:c.720+69A= ENSP00000508955.1:n.720+69A=
ENST00000691229.1:c.720+69A= ENSP00000510437.1:n.720+69A=
ENST00000692089.1:c.720+69A= ENSP00000508626.1:n.720+69A=
XM_005264515.3:c.720+69A= XP_005264572.1:n.720+69A=
XM_005264515.4:c.720+69A= XP_005264572.1:n.720+69A=
XM_011533060.1:c.813+69A= XP_011531362.1:n.813+69A=
XM_011533061.1:c.813+69A= XP_011531363.1:n.813+69A=
XM_011533062.1:c.699+69A= XP_011531364.1:n.699+69A=
XM_011533062.2:c.699+69A= XP_011531364.1:n.699+69A=
XM_011533063.1:c.696+69A= XP_011531365.1:n.696+69A=
XM_011533064.1:c.549+69A= XP_011531366.1:n.549+69A=
XM_011533064.2:c.549+69A= XP_011531366.1:n.549+69A=
XM_011533065.1:c.813+69A= XP_011531367.1:n.813+69A=
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