Canonical Allele Identifier: CA347725
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 161102
ClinVar RCV Id: RCV000202473
dbSNP Id: rs753723351

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726909G>A , CM000682.2:g.46726909G>A GRCh38
NC_000020.10:g.45355548G>A , CM000682.1:g.45355548G>A GRCh37
NC_000020.9:g.44788955G>A NCBI36
NG_016284.1:g.22270G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1334G>A MANE Select ENSP00000352216.2:p.Gly445Glu
ENST00000359271.3:c.1334G>A ENSP00000352216.2:p.Gly445Glu
NM_030777.3:c.1334G>A NP_110404.1:p.Gly445Glu
XM_011529060.1:c.1397G>A XP_011527362.1:p.Gly466Glu
XM_011529061.1:c.1343G>A XP_011527363.1:p.Gly448Glu
XM_011529062.1:c.1446G>A XP_011527364.1:p.Arg482=
XM_011529063.1:c.1397G>A XP_011527365.1:p.Gly466Glu
XM_011529064.1:c.1446G>A XP_011527366.1:p.Arg482=
XM_011529065.1:c.1397G>A XP_011527367.1:p.Gly466Glu
XR_936641.1:n.1582G>A
XM_011529060.2:c.1397G>A XP_011527362.1:p.Gly466Glu
XM_011529061.2:c.1343G>A XP_011527363.1:p.Gly448Glu
XM_011529062.2:c.1446G>A XP_011527364.1:p.Arg482=
XM_011529063.2:c.1397G>A XP_011527365.1:p.Gly466Glu
XM_011529064.2:c.1446G>A XP_011527366.1:p.Arg482=
XM_011529065.2:c.1397G>A XP_011527367.1:p.Gly466Glu
XM_017028087.2:c.1334G>A XP_016883576.1:p.Gly445Glu
XR_936641.2:n.1569G>A
NM_030777.4:c.1334G>A MANE Select NP_110404.1:p.Gly445Glu