Canonical Allele Identifier: CA7177301

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50160019C>T , CM000676.2:g.50160019C>T	GRCh38
NC_000014.8:g.50626737C>T , CM000676.1:g.50626737C>T	GRCh37
NC_000014.7:g.49696487C>T	NCBI36
NG_051073.1:g.76675G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.1264G>A MANE Select	NP_008870.2:p.Glu422Lys
ENST00000216373.10:c.1264G>A MANE Select	ENSP00000216373.5:p.Glu422Lys
NM_006939.2:c.1264G>A	NP_008870.2:p.Glu422Lys
NM_006939.3:c.1264G>A	NP_008870.2:p.Glu422Lys
ENST00000216373.9:c.1264G>A	ENSP00000216373.5:p.Glu422Lys
ENST00000543680.5:c.1165G>A	ENSP00000445328.1:p.Glu389Lys
ENST00000555794.2:c.378G>A
XM_005268021.1:c.1084G>A	XP_005268078.1:p.Glu362Lys
XM_011537103.1:c.1225G>A	XP_011535405.1:p.Glu409Lys
XM_011537104.1:c.1264G>A	XP_011535406.1:p.Glu422Lys