Canonical Allele Identifier: CA409266491
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725209C>A , CM000682.2:g.46725209C>A GRCh38
NC_000020.10:g.45353848C>A , CM000682.1:g.45353848C>A GRCh37
NC_000020.9:g.44787255C>A NCBI36
NG_016284.1:g.20570C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.173C>A MANE Select ENSP00000352216.2:p.Ala58Asp
ENST00000359271.3:c.173C>A ENSP00000352216.2:p.Ala58Asp
ENST00000611837.1:n.325C>A
NM_030777.3:c.173C>A NP_110404.1:p.Ala58Asp
XM_011529060.1:c.236C>A XP_011527362.1:p.Ala79Asp
XM_011529061.1:c.182C>A XP_011527363.1:p.Ala61Asp
XM_011529062.1:c.236C>A XP_011527364.1:p.Ala79Asp
XM_011529063.1:c.236C>A XP_011527365.1:p.Ala79Asp
XM_011529064.1:c.236C>A XP_011527366.1:p.Ala79Asp
XM_011529065.1:c.236C>A XP_011527367.1:p.Ala79Asp
XR_936641.1:n.372C>A
XM_011529060.2:c.236C>A XP_011527362.1:p.Ala79Asp
XM_011529061.2:c.182C>A XP_011527363.1:p.Ala61Asp
XM_011529062.2:c.236C>A XP_011527364.1:p.Ala79Asp
XM_011529063.2:c.236C>A XP_011527365.1:p.Ala79Asp
XM_011529064.2:c.236C>A XP_011527366.1:p.Ala79Asp
XM_011529065.2:c.236C>A XP_011527367.1:p.Ala79Asp
XM_017028087.2:c.173C>A XP_016883576.1:p.Ala58Asp
XR_936641.2:n.359C>A
NM_030777.4:c.173C>A MANE Select NP_110404.1:p.Ala58Asp