Canonical Allele Identifier: CA9891955

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725358G>A , CM000682.2:g.46725358G>A	GRCh38
NC_000020.10:g.45353997G>A , CM000682.1:g.45353997G>A	GRCh37
NC_000020.9:g.44787404G>A	NCBI36
NG_016284.1:g.20719G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.322G>A MANE Select	NP_110404.1:p.Val108Ile
ENST00000359271.4:c.322G>A MANE Select	ENSP00000352216.2:p.Val108Ile
NM_030777.3:c.322G>A	NP_110404.1:p.Val108Ile
ENST00000359271.3:c.322G>A	ENSP00000352216.2:p.Val108Ile
ENST00000611837.1:n.474G>A
XM_011529060.1:c.385G>A	XP_011527362.1:p.Val129Ile
XM_011529060.2:c.385G>A	XP_011527362.1:p.Val129Ile
XM_011529061.1:c.331G>A	XP_011527363.1:p.Val111Ile
XM_011529061.2:c.331G>A	XP_011527363.1:p.Val111Ile
XM_011529062.1:c.385G>A	XP_011527364.1:p.Val129Ile
XM_011529062.2:c.385G>A	XP_011527364.1:p.Val129Ile
XM_011529063.1:c.385G>A	XP_011527365.1:p.Val129Ile
XM_011529063.2:c.385G>A	XP_011527365.1:p.Val129Ile
XM_011529064.1:c.385G>A	XP_011527366.1:p.Val129Ile
XM_011529064.2:c.385G>A	XP_011527366.1:p.Val129Ile
XM_011529065.1:c.385G>A	XP_011527367.1:p.Val129Ile
XM_011529065.2:c.385G>A	XP_011527367.1:p.Val129Ile
XM_017028087.2:c.322G>A	XP_016883576.1:p.Val108Ile
XR_936641.1:n.521G>A
XR_936641.2:n.508G>A