Canonical Allele Identifier: CA7177273

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50159775T>A , CM000676.2:g.50159775T>A	GRCh38
NC_000014.8:g.50626493T>A , CM000676.1:g.50626493T>A	GRCh37
NC_000014.7:g.49696243T>A	NCBI36
NG_051073.1:g.76919A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.1508A>T MANE Select	NP_008870.2:p.Glu503Val
ENST00000216373.10:c.1508A>T MANE Select	ENSP00000216373.5:p.Glu503Val
NM_006939.2:c.1508A>T	NP_008870.2:p.Glu503Val
NM_006939.3:c.1508A>T	NP_008870.2:p.Glu503Val
ENST00000216373.9:c.1508A>T	ENSP00000216373.5:p.Glu503Val
ENST00000543680.5:c.1409A>T	ENSP00000445328.1:p.Glu470Val
ENST00000555794.2:c.622A>T
XM_005268021.1:c.1328A>T	XP_005268078.1:p.Glu443Val
XM_011537103.1:c.1469A>T	XP_011535405.1:p.Glu490Val
XM_011537104.1:c.1508A>T	XP_011535406.1:p.Glu503Val