Canonical Allele Identifier: CA409267034
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725488A>T , CM000682.2:g.46725488A>T GRCh38
NC_000020.10:g.45354127A>T , CM000682.1:g.45354127A>T GRCh37
NC_000020.9:g.44787534A>T NCBI36
NG_016284.1:g.20849A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.452A>T MANE Select ENSP00000352216.2:p.Tyr151Phe
ENST00000359271.3:c.452A>T ENSP00000352216.2:p.Tyr151Phe
NM_030777.3:c.452A>T NP_110404.1:p.Tyr151Phe
XM_011529060.1:c.515A>T XP_011527362.1:p.Tyr172Phe
XM_011529061.1:c.461A>T XP_011527363.1:p.Tyr154Phe
XM_011529062.1:c.515A>T XP_011527364.1:p.Tyr172Phe
XM_011529063.1:c.515A>T XP_011527365.1:p.Tyr172Phe
XM_011529064.1:c.515A>T XP_011527366.1:p.Tyr172Phe
XM_011529065.1:c.515A>T XP_011527367.1:p.Tyr172Phe
XR_936641.1:n.651A>T
XM_011529060.2:c.515A>T XP_011527362.1:p.Tyr172Phe
XM_011529061.2:c.461A>T XP_011527363.1:p.Tyr154Phe
XM_011529062.2:c.515A>T XP_011527364.1:p.Tyr172Phe
XM_011529063.2:c.515A>T XP_011527365.1:p.Tyr172Phe
XM_011529064.2:c.515A>T XP_011527366.1:p.Tyr172Phe
XM_011529065.2:c.515A>T XP_011527367.1:p.Tyr172Phe
XM_017028087.2:c.452A>T XP_016883576.1:p.Tyr151Phe
XR_936641.2:n.638A>T
NM_030777.4:c.452A>T MANE Select NP_110404.1:p.Tyr151Phe