Canonical Allele Identifier: CA241805
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 195383
dbSNP Id: rs143301610

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725551C>T , CM000682.2:g.46725551C>T GRCh38
NC_000020.10:g.45354190C>T , CM000682.1:g.45354190C>T GRCh37
NC_000020.9:g.44787597C>T NCBI36
NG_016284.1:g.20912C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.515C>T MANE Select ENSP00000352216.2:p.Thr172Ile
ENST00000359271.3:c.515C>T ENSP00000352216.2:p.Thr172Ile
NM_030777.3:c.515C>T NP_110404.1:p.Thr172Ile
XM_011529060.1:c.578C>T XP_011527362.1:p.Thr193Ile
XM_011529061.1:c.524C>T XP_011527363.1:p.Thr175Ile
XM_011529062.1:c.578C>T XP_011527364.1:p.Thr193Ile
XM_011529063.1:c.578C>T XP_011527365.1:p.Thr193Ile
XM_011529064.1:c.578C>T XP_011527366.1:p.Thr193Ile
XM_011529065.1:c.578C>T XP_011527367.1:p.Thr193Ile
XR_936641.1:n.714C>T
XM_011529060.2:c.578C>T XP_011527362.1:p.Thr193Ile
XM_011529061.2:c.524C>T XP_011527363.1:p.Thr175Ile
XM_011529062.2:c.578C>T XP_011527364.1:p.Thr193Ile
XM_011529063.2:c.578C>T XP_011527365.1:p.Thr193Ile
XM_011529064.2:c.578C>T XP_011527366.1:p.Thr193Ile
XM_011529065.2:c.578C>T XP_011527367.1:p.Thr193Ile
XM_017028087.2:c.515C>T XP_016883576.1:p.Thr172Ile
XR_936641.2:n.701C>T
NM_030777.4:c.515C>T MANE Select NP_110404.1:p.Thr172Ile