Canonical Allele Identifier: CA2136084577

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180583G= , CM000676.2:g.50180583G=	GRCh38
NC_000014.8:g.50647301G= , CM000676.1:g.50647301G=	GRCh37
NC_000014.7:g.49717051G=	NCBI36
NG_051073.1:g.56111C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.958C= MANE Select	ENSP00000216373.5:p.Leu320=
ENST00000216373.9:c.958C=	ENSP00000216373.5:p.Leu320=
ENST00000543680.5:c.958C=	ENSP00000445328.1:p.Leu320=
ENST00000555794.2:c.72C=
NM_006939.2:c.958C=	NP_008870.2:p.Leu320=
XM_005268021.1:c.778C=	XP_005268078.1:p.Leu260=
XM_011537103.1:c.919C=	XP_011535405.1:p.Leu307=
XM_011537104.1:c.958C=	XP_011535406.1:p.Leu320=
XR_943842.1:n.954-3204G=
XR_943843.1:n.954-3204G=
NM_006939.3:c.958C=	NP_008870.2:p.Leu320=
NM_006939.4:c.958C= MANE Select	NP_008870.2:p.Leu320=