Canonical Allele Identifier: CA2136084616

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180608T= , CM000676.2:g.50180608T=	GRCh38
NC_000014.8:g.50647326T= , CM000676.1:g.50647326T=	GRCh37
NC_000014.7:g.49717076T=	NCBI36
NG_051073.1:g.56086A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.933A= MANE Select	ENSP00000216373.5:p.Lys311=
ENST00000216373.9:c.933A=	ENSP00000216373.5:p.Lys311=
ENST00000543680.5:c.933A=	ENSP00000445328.1:p.Lys311=
ENST00000555794.2:c.47A=
NM_006939.2:c.933A=	NP_008870.2:p.Lys311=
XM_005268021.1:c.753A=	XP_005268078.1:p.Lys251=
XM_011537103.1:c.894A=	XP_011535405.1:p.Lys298=
XM_011537104.1:c.933A=	XP_011535406.1:p.Lys311=
XR_943842.1:n.954-3179T=
XR_943843.1:n.954-3179T=
NM_006939.3:c.933A=	NP_008870.2:p.Lys311=
NM_006939.4:c.933A= MANE Select	NP_008870.2:p.Lys311=