Canonical Allele Identifier: CA2136094894

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199744G= , CM000676.2:g.50199744G=	GRCh38
NC_000014.8:g.50666462G= , CM000676.1:g.50666462G=	GRCh37
NC_000014.7:g.49736212G=	NCBI36
NG_051073.1:g.36950C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.457C= MANE Select	ENSP00000216373.5:p.Arg153=
ENST00000216373.9:c.457C=	ENSP00000216373.5:p.Arg153=
ENST00000543680.5:c.457C=	ENSP00000445328.1:p.Arg153=
ENST00000555666.1:n.636C=
ENST00000556469.5:n.428C=
NM_006939.2:c.457C=	NP_008870.2:p.Arg153=
XM_005268021.1:c.277C=	XP_005268078.1:p.Arg93=
XM_011537103.1:c.418C=	XP_011535405.1:p.Arg140=
XM_011537104.1:c.457C=	XP_011535406.1:p.Arg153=
XR_943842.1:n.1039+15872G=
XR_943843.1:n.1039+15872G=
NM_006939.3:c.457C=	NP_008870.2:p.Arg153=
NM_006939.4:c.457C= MANE Select	NP_008870.2:p.Arg153=