Canonical Allele Identifier: CA9892009
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 263561
dbSNP Id: rs755339268

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725646G>A , CM000682.2:g.46725646G>A GRCh38
NC_000020.10:g.45354285G>A , CM000682.1:g.45354285G>A GRCh37
NC_000020.9:g.44787692G>A NCBI36
NG_016284.1:g.21007G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.610G>A MANE Select ENSP00000352216.2:p.Gly204Ser
ENST00000359271.3:c.610G>A ENSP00000352216.2:p.Gly204Ser
NM_030777.3:c.610G>A NP_110404.1:p.Gly204Ser
XM_011529060.1:c.673G>A XP_011527362.1:p.Gly225Ser
XM_011529061.1:c.619G>A XP_011527363.1:p.Gly207Ser
XM_011529062.1:c.673G>A XP_011527364.1:p.Gly225Ser
XM_011529063.1:c.673G>A XP_011527365.1:p.Gly225Ser
XM_011529064.1:c.673G>A XP_011527366.1:p.Gly225Ser
XM_011529065.1:c.673G>A XP_011527367.1:p.Gly225Ser
XR_936641.1:n.809G>A
XM_011529060.2:c.673G>A XP_011527362.1:p.Gly225Ser
XM_011529061.2:c.619G>A XP_011527363.1:p.Gly207Ser
XM_011529062.2:c.673G>A XP_011527364.1:p.Gly225Ser
XM_011529063.2:c.673G>A XP_011527365.1:p.Gly225Ser
XM_011529064.2:c.673G>A XP_011527366.1:p.Gly225Ser
XM_011529065.2:c.673G>A XP_011527367.1:p.Gly225Ser
XM_017028087.2:c.610G>A XP_016883576.1:p.Gly204Ser
XR_936641.2:n.796G>A
NM_030777.4:c.610G>A MANE Select NP_110404.1:p.Gly204Ser