Canonical Allele Identifier: CA324057
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 213737
dbSNP Id: rs201393026

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726945C>T , CM000682.2:g.46726945C>T GRCh38
NC_000020.10:g.45355584C>T , CM000682.1:g.45355584C>T GRCh37
NC_000020.9:g.44788991C>T NCBI36
NG_016284.1:g.22306C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1370C>T MANE Select ENSP00000352216.2:p.Ala457Val
ENST00000359271.3:c.1370C>T ENSP00000352216.2:p.Ala457Val
NM_030777.3:c.1370C>T NP_110404.1:p.Ala457Val
XM_011529060.1:c.1433C>T XP_011527362.1:p.Ala478Val
XM_011529061.1:c.1379C>T XP_011527363.1:p.Ala460Val
XM_011529062.1:c.1482C>T XP_011527364.1:p.Gly494=
XM_011529063.1:c.1433C>T XP_011527365.1:p.Ala478Val
XM_011529064.1:c.1482C>T XP_011527366.1:p.Gly494=
XM_011529065.1:c.1433C>T XP_011527367.1:p.Ala478Val
XR_936641.1:n.1618C>T
XM_011529060.2:c.1433C>T XP_011527362.1:p.Ala478Val
XM_011529061.2:c.1379C>T XP_011527363.1:p.Ala460Val
XM_011529062.2:c.1482C>T XP_011527364.1:p.Gly494=
XM_011529063.2:c.1433C>T XP_011527365.1:p.Ala478Val
XM_011529064.2:c.1482C>T XP_011527366.1:p.Gly494=
XM_011529065.2:c.1433C>T XP_011527367.1:p.Ala478Val
XM_017028087.2:c.1370C>T XP_016883576.1:p.Ala457Val
XR_936641.2:n.1605C>T
NM_030777.4:c.1370C>T MANE Select NP_110404.1:p.Ala457Val