Canonical Allele Identifier: CA2136084578

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180584A= , CM000676.2:g.50180584A=	GRCh38
NC_000014.8:g.50647302A= , CM000676.1:g.50647302A=	GRCh37
NC_000014.7:g.49717052A=	NCBI36
NG_051073.1:g.56110T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.957T= MANE Select	ENSP00000216373.5:p.Ala319=
ENST00000216373.9:c.957T=	ENSP00000216373.5:p.Ala319=
ENST00000543680.5:c.957T=	ENSP00000445328.1:p.Ala319=
ENST00000555794.2:c.71T=
NM_006939.2:c.957T=	NP_008870.2:p.Ala319=
XM_005268021.1:c.777T=	XP_005268078.1:p.Ala259=
XM_011537103.1:c.918T=	XP_011535405.1:p.Ala306=
XM_011537104.1:c.957T=	XP_011535406.1:p.Ala319=
XR_943842.1:n.954-3203A=
XR_943843.1:n.954-3203A=
NM_006939.3:c.957T=	NP_008870.2:p.Ala319=
NM_006939.4:c.957T= MANE Select	NP_008870.2:p.Ala319=