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: CA1246153612
Community Standard Title: NM_005633.4(SOS1):c.720+77C=
Gene: SOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39054537G= , CM000664.2:g.39054537G= GRCh38
NC_000002.11:g.39281678G= , CM000664.1:g.39281678G= GRCh37
NC_000002.10:g.39135182G= NCBI36
NG_007530.1:g.70927C= , LRG_754:g.70927C=

Transcript Alleles

HGVS Amino-acid Change
NM_005633.4:c.720+77C= MANE Select NP_005624.2:n.720+77C=
ENST00000402219.8:c.720+77C= MANE Select ENSP00000384675.2:n.720+77C=
NM_001382394.1:c.699+77C= NP_001369323.1:n.699+77C=
NM_001382395.1:c.720+77C= NP_001369324.1:n.720+77C=
NM_005633.3:c.720+77C= , LRG_754t1:c.720+77C= NP_005624.2:n.720+77C=
ENST00000395038.6:c.720+77C= ENSP00000378479.2:n.720+77C=
ENST00000402219.6:c.720+77C= ENSP00000384675.2:n.720+77C=
ENST00000426016.5:c.720+77C= ENSP00000387784.1:n.720+77C=
ENST00000461545.2:n.747+77C=
ENST00000685782.1:n.1558+77C=
ENST00000688189.1:n.562C=
ENST00000689668.1:n.727+77C=
ENST00000690679.1:c.820+77C=
ENST00000690876.1:c.720+77C= ENSP00000508955.1:n.720+77C=
ENST00000691229.1:c.720+77C= ENSP00000510437.1:n.720+77C=
ENST00000692089.1:c.720+77C= ENSP00000508626.1:n.720+77C=
XM_005264515.3:c.720+77C= XP_005264572.1:n.720+77C=
XM_005264515.4:c.720+77C= XP_005264572.1:n.720+77C=
XM_011533060.1:c.813+77C= XP_011531362.1:n.813+77C=
XM_011533061.1:c.813+77C= XP_011531363.1:n.813+77C=
XM_011533062.1:c.699+77C= XP_011531364.1:n.699+77C=
XM_011533062.2:c.699+77C= XP_011531364.1:n.699+77C=
XM_011533063.1:c.696+77C= XP_011531365.1:n.696+77C=
XM_011533064.1:c.549+77C= XP_011531366.1:n.549+77C=
XM_011533064.2:c.549+77C= XP_011531366.1:n.549+77C=
XM_011533065.1:c.813+77C= XP_011531367.1:n.813+77C=
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