Canonical Allele Identifier: CA9892048

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725844G>A , CM000682.2:g.46725844G>A	GRCh38
NC_000020.10:g.45354483G>A , CM000682.1:g.45354483G>A	GRCh37
NC_000020.9:g.44787890G>A	NCBI36
NG_016284.1:g.21205G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.808G>A MANE Select	NP_110404.1:p.Val270Met
ENST00000359271.4:c.808G>A MANE Select	ENSP00000352216.2:p.Val270Met
NM_030777.3:c.808G>A	NP_110404.1:p.Val270Met
ENST00000359271.3:c.808G>A	ENSP00000352216.2:p.Val270Met
XM_011529060.1:c.871G>A	XP_011527362.1:p.Val291Met
XM_011529060.2:c.871G>A	XP_011527362.1:p.Val291Met
XM_011529061.1:c.817G>A	XP_011527363.1:p.Val273Met
XM_011529061.2:c.817G>A	XP_011527363.1:p.Val273Met
XM_011529062.1:c.871G>A	XP_011527364.1:p.Val291Met
XM_011529062.2:c.871G>A	XP_011527364.1:p.Val291Met
XM_011529063.1:c.871G>A	XP_011527365.1:p.Val291Met
XM_011529063.2:c.871G>A	XP_011527365.1:p.Val291Met
XM_011529064.1:c.871G>A	XP_011527366.1:p.Val291Met
XM_011529064.2:c.871G>A	XP_011527366.1:p.Val291Met
XM_011529065.1:c.871G>A	XP_011527367.1:p.Val291Met
XM_011529065.2:c.871G>A	XP_011527367.1:p.Val291Met
XM_017028087.2:c.808G>A	XP_016883576.1:p.Val270Met
XR_936641.1:n.1007G>A
XR_936641.2:n.994G>A