Canonical Allele Identifier: CA2136094925

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199841G= , CM000676.2:g.50199841G=	GRCh38
NC_000014.8:g.50666559G= , CM000676.1:g.50666559G=	GRCh37
NC_000014.7:g.49736309G=	NCBI36
NG_051073.1:g.36853C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.360C= MANE Select	ENSP00000216373.5:p.Tyr120=
ENST00000216373.9:c.360C=	ENSP00000216373.5:p.Tyr120=
ENST00000543680.5:c.360C=	ENSP00000445328.1:p.Tyr120=
ENST00000555666.1:n.539C=
ENST00000556469.5:n.331C=
NM_006939.2:c.360C=	NP_008870.2:p.Tyr120=
XM_005268021.1:c.180C=	XP_005268078.1:p.Tyr60=
XM_011537103.1:c.321C=	XP_011535405.1:p.Tyr107=
XM_011537104.1:c.360C=	XP_011535406.1:p.Tyr120=
XR_943842.1:n.1039+15969G=
XR_943843.1:n.1039+15969G=
NM_006939.3:c.360C=	NP_008870.2:p.Tyr120=
NM_006939.4:c.360C= MANE Select	NP_008870.2:p.Tyr120=