Canonical Allele Identifier: CA1246128904

Gene: SOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39007168C= , CM000664.2:g.39007168C=	GRCh38
NC_000002.11:g.39234309C= , CM000664.1:g.39234309C=	GRCh37
NC_000002.10:g.39087813C=	NCBI36
NG_007530.1:g.118296G= , LRG_754:g.118296G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685279.1:c.1303G=	ENSP00000509424.1:p.Glu435=
ENST00000689668.1:n.2543G=
ENST00000690876.1:c.2425G=	ENSP00000508955.1:p.Glu809=
ENST00000691229.1:c.2305G=	ENSP00000510437.1:p.Glu769=
ENST00000692089.1:c.2425G=	ENSP00000508626.1:p.Glu809=
ENST00000692227.1:c.232G=	ENSP00000509138.1:p.Glu78=
ENST00000692620.1:c.*123G=	ENSP00000509311.1:n.*123G=
ENST00000402219.8:c.2536G= MANE Select	ENSP00000384675.2:p.Glu846=
ENST00000395038.6:c.2536G=	ENSP00000378479.2:p.Glu846=
ENST00000402219.6:c.2536G=	ENSP00000384675.2:p.Glu846=
ENST00000426016.5:c.2536G=	ENSP00000387784.1:p.Glu846=
ENST00000474390.1:n.332G=
NM_005633.3:c.2536G= , LRG_754t1:c.2536G=	NP_005624.2:p.Glu846=
XM_005264515.3:c.2536G=	XP_005264572.1:p.Glu846=
XM_011533060.1:c.2629G=	XP_011531362.1:p.Glu877=
XM_011533061.1:c.2629G=	XP_011531363.1:p.Glu877=
XM_011533062.1:c.2515G=	XP_011531364.1:p.Glu839=
XM_011533063.1:c.2512G=	XP_011531365.1:p.Glu838=
XM_011533064.1:c.2365G=	XP_011531366.1:p.Glu789=
XM_011533065.1:c.2629G=	XP_011531367.1:p.Glu877=
XM_011533066.1:c.1471G=	XP_011531368.1:p.Glu491=
XM_005264515.4:c.2536G=	XP_005264572.1:p.Glu846=
XM_011533062.2:c.2515G=	XP_011531364.1:p.Glu839=
XM_011533064.2:c.2365G=	XP_011531366.1:p.Glu789=
NM_001382394.1:c.2515G=	NP_001369323.1:p.Glu839=
NM_001382395.1:c.2536G=	NP_001369324.1:p.Glu846=
NM_005633.4:c.2536G= MANE Select	NP_005624.2:p.Glu846=