Canonical Allele Identifier: CA2136094910

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199804C= , CM000676.2:g.50199804C=	GRCh38
NC_000014.8:g.50666522C= , CM000676.1:g.50666522C=	GRCh37
NC_000014.7:g.49736272C=	NCBI36
NG_051073.1:g.36890G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.397G= MANE Select	ENSP00000216373.5:p.Val133=
ENST00000216373.9:c.397G=	ENSP00000216373.5:p.Val133=
ENST00000543680.5:c.397G=	ENSP00000445328.1:p.Val133=
ENST00000555666.1:n.576G=
ENST00000556469.5:n.368G=
NM_006939.2:c.397G=	NP_008870.2:p.Val133=
XM_005268021.1:c.217G=	XP_005268078.1:p.Val73=
XM_011537103.1:c.358G=	XP_011535405.1:p.Val120=
XM_011537104.1:c.397G=	XP_011535406.1:p.Val133=
XR_943842.1:n.1039+15932C=
XR_943843.1:n.1039+15932C=
NM_006939.3:c.397G=	NP_008870.2:p.Val133=
NM_006939.4:c.397G= MANE Select	NP_008870.2:p.Val133=