Canonical Allele Identifier: CA409266623
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725271C>T , CM000682.2:g.46725271C>T GRCh38
NC_000020.10:g.45353910C>T , CM000682.1:g.45353910C>T GRCh37
NC_000020.9:g.44787317C>T NCBI36
NG_016284.1:g.20632C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.235C>T MANE Select ENSP00000352216.2:p.Leu79Phe
ENST00000359271.3:c.235C>T ENSP00000352216.2:p.Leu79Phe
ENST00000611837.1:n.387C>T
NM_030777.3:c.235C>T NP_110404.1:p.Leu79Phe
XM_011529060.1:c.298C>T XP_011527362.1:p.Leu100Phe
XM_011529061.1:c.244C>T XP_011527363.1:p.Leu82Phe
XM_011529062.1:c.298C>T XP_011527364.1:p.Leu100Phe
XM_011529063.1:c.298C>T XP_011527365.1:p.Leu100Phe
XM_011529064.1:c.298C>T XP_011527366.1:p.Leu100Phe
XM_011529065.1:c.298C>T XP_011527367.1:p.Leu100Phe
XR_936641.1:n.434C>T
XM_011529060.2:c.298C>T XP_011527362.1:p.Leu100Phe
XM_011529061.2:c.244C>T XP_011527363.1:p.Leu82Phe
XM_011529062.2:c.298C>T XP_011527364.1:p.Leu100Phe
XM_011529063.2:c.298C>T XP_011527365.1:p.Leu100Phe
XM_011529064.2:c.298C>T XP_011527366.1:p.Leu100Phe
XM_011529065.2:c.298C>T XP_011527367.1:p.Leu100Phe
XM_017028087.2:c.235C>T XP_016883576.1:p.Leu79Phe
XR_936641.2:n.421C>T
NM_030777.4:c.235C>T MANE Select NP_110404.1:p.Leu79Phe