Canonical Allele Identifier: CA9891984
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs767213709

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725518C>A , CM000682.2:g.46725518C>A GRCh38
NC_000020.10:g.45354157C>A , CM000682.1:g.45354157C>A GRCh37
NC_000020.9:g.44787564C>A NCBI36
NG_016284.1:g.20879C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.482C>A MANE Select ENSP00000352216.2:p.Pro161His
ENST00000359271.3:c.482C>A ENSP00000352216.2:p.Pro161His
NM_030777.3:c.482C>A NP_110404.1:p.Pro161His
XM_011529060.1:c.545C>A XP_011527362.1:p.Pro182His
XM_011529061.1:c.491C>A XP_011527363.1:p.Pro164His
XM_011529062.1:c.545C>A XP_011527364.1:p.Pro182His
XM_011529063.1:c.545C>A XP_011527365.1:p.Pro182His
XM_011529064.1:c.545C>A XP_011527366.1:p.Pro182His
XM_011529065.1:c.545C>A XP_011527367.1:p.Pro182His
XR_936641.1:n.681C>A
XM_011529060.2:c.545C>A XP_011527362.1:p.Pro182His
XM_011529061.2:c.491C>A XP_011527363.1:p.Pro164His
XM_011529062.2:c.545C>A XP_011527364.1:p.Pro182His
XM_011529063.2:c.545C>A XP_011527365.1:p.Pro182His
XM_011529064.2:c.545C>A XP_011527366.1:p.Pro182His
XM_011529065.2:c.545C>A XP_011527367.1:p.Pro182His
XM_017028087.2:c.482C>A XP_016883576.1:p.Pro161His
XR_936641.2:n.668C>A
NM_030777.4:c.482C>A MANE Select NP_110404.1:p.Pro161His