Canonical Allele Identifier: CA2136094912

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199810C= , CM000676.2:g.50199810C=	GRCh38
NC_000014.8:g.50666528C= , CM000676.1:g.50666528C=	GRCh37
NC_000014.7:g.49736278C=	NCBI36
NG_051073.1:g.36884G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.391G= MANE Select	ENSP00000216373.5:p.Val131=
ENST00000216373.9:c.391G=	ENSP00000216373.5:p.Val131=
ENST00000543680.5:c.391G=	ENSP00000445328.1:p.Val131=
ENST00000555666.1:n.570G=
ENST00000556469.5:n.362G=
NM_006939.2:c.391G=	NP_008870.2:p.Val131=
XM_005268021.1:c.211G=	XP_005268078.1:p.Val71=
XM_011537103.1:c.352G=	XP_011535405.1:p.Val118=
XM_011537104.1:c.391G=	XP_011535406.1:p.Val131=
XR_943842.1:n.1039+15938C=
XR_943843.1:n.1039+15938C=
NM_006939.3:c.391G=	NP_008870.2:p.Val131=
NM_006939.4:c.391G= MANE Select	NP_008870.2:p.Val131=