Canonical Allele Identifier: CA409266782

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45353998T>A (hg19) ; chr20:g.46725359T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725359T>A , CM000682.2:g.46725359T>A	GRCh38
NC_000020.10:g.45353998T>A , CM000682.1:g.45353998T>A	GRCh37
NC_000020.9:g.44787405T>A	NCBI36
NG_016284.1:g.20720T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.323T>A MANE Select	ENSP00000352216.2:p.Val108Asp
ENST00000359271.3:c.323T>A	ENSP00000352216.2:p.Val108Asp
ENST00000611837.1:n.475T>A
NM_030777.3:c.323T>A	NP_110404.1:p.Val108Asp
XM_011529060.1:c.386T>A	XP_011527362.1:p.Val129Asp
XM_011529061.1:c.332T>A	XP_011527363.1:p.Val111Asp
XM_011529062.1:c.386T>A	XP_011527364.1:p.Val129Asp
XM_011529063.1:c.386T>A	XP_011527365.1:p.Val129Asp
XM_011529064.1:c.386T>A	XP_011527366.1:p.Val129Asp
XM_011529065.1:c.386T>A	XP_011527367.1:p.Val129Asp
XR_936641.1:n.522T>A
XM_011529060.2:c.386T>A	XP_011527362.1:p.Val129Asp
XM_011529061.2:c.332T>A	XP_011527363.1:p.Val111Asp
XM_011529062.2:c.386T>A	XP_011527364.1:p.Val129Asp
XM_011529063.2:c.386T>A	XP_011527365.1:p.Val129Asp
XM_011529064.2:c.386T>A	XP_011527366.1:p.Val129Asp
XM_011529065.2:c.386T>A	XP_011527367.1:p.Val129Asp
XM_017028087.2:c.323T>A	XP_016883576.1:p.Val108Asp
XR_936641.2:n.509T>A
NM_030777.4:c.323T>A MANE Select	NP_110404.1:p.Val108Asp