Canonical Allele Identifier: CA340267
Gene: SLC2A10 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 4590
dbSNP Id: rs121908173

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725430C>T , CM000682.2:g.46725430C>T GRCh38
NC_000020.10:g.45354069C>T , CM000682.1:g.45354069C>T GRCh37
NC_000020.9:g.44787476C>T NCBI36
NG_016284.1:g.20791C>T

Transcript Alleles

HGVS Amino-acid change
NM_030777.3:c.394C>T VV NP_110404.1:p.Arg132Trp
XM_011529060.1:c.457C>T XP_011527362.1:p.Arg153Trp
XM_011529061.1:c.403C>T XP_011527363.1:p.Arg135Trp
XM_011529062.1:c.457C>T XP_011527364.1:p.Arg153Trp
XM_011529063.1:c.457C>T XP_011527365.1:p.Arg153Trp
XM_011529064.1:c.457C>T XP_011527366.1:p.Arg153Trp
XM_011529065.1:c.457C>T XP_011527367.1:p.Arg153Trp
XR_936641.1:n.593C>T
XM_011529060.2:c.457C>T
XM_011529061.2:c.403C>T
XM_011529062.2:c.457C>T
XM_011529063.2:c.457C>T
XM_011529064.2:c.457C>T
XM_011529065.2:c.457C>T
XM_017028087.2:c.394C>T XP_016883576.1:p.Arg132Trp
XR_936641.2:n.580C>T
ENST00000359271.3:c.394C>T ENSP00000352216.2:p.Arg132Trp
ENST00000611837.1:n.546C>T