Canonical Allele Identifier: CA2136084613

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180607A= , CM000676.2:g.50180607A=	GRCh38
NC_000014.8:g.50647325A= , CM000676.1:g.50647325A=	GRCh37
NC_000014.7:g.49717075A=	NCBI36
NG_051073.1:g.56087T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.934T= MANE Select	ENSP00000216373.5:p.Leu312=
ENST00000216373.9:c.934T=	ENSP00000216373.5:p.Leu312=
ENST00000543680.5:c.934T=	ENSP00000445328.1:p.Leu312=
ENST00000555794.2:c.48T=
NM_006939.2:c.934T=	NP_008870.2:p.Leu312=
XM_005268021.1:c.754T=	XP_005268078.1:p.Leu252=
XM_011537103.1:c.895T=	XP_011535405.1:p.Leu299=
XM_011537104.1:c.934T=	XP_011535406.1:p.Leu312=
XR_943842.1:n.954-3180A=
XR_943843.1:n.954-3180A=
NM_006939.3:c.934T=	NP_008870.2:p.Leu312=
NM_006939.4:c.934T= MANE Select	NP_008870.2:p.Leu312=