Canonical Allele Identifier: CA409266431
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725178G>T , CM000682.2:g.46725178G>T GRCh38
NC_000020.10:g.45353817G>T , CM000682.1:g.45353817G>T GRCh37
NC_000020.9:g.44787224G>T NCBI36
NG_016284.1:g.20539G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359271.4:c.142G>T MANE Select ENSP00000352216.2:p.Glu48Ter
ENST00000359271.3:c.142G>T ENSP00000352216.2:p.Glu48Ter
ENST00000611837.1:n.294G>T
NM_030777.3:c.142G>T NP_110404.1:p.Glu48Ter
XM_011529060.1:c.205G>T XP_011527362.1:p.Glu69Ter
XM_011529061.1:c.151G>T XP_011527363.1:p.Glu51Ter
XM_011529062.1:c.205G>T XP_011527364.1:p.Glu69Ter
XM_011529063.1:c.205G>T XP_011527365.1:p.Glu69Ter
XM_011529064.1:c.205G>T XP_011527366.1:p.Glu69Ter
XM_011529065.1:c.205G>T XP_011527367.1:p.Glu69Ter
XR_936641.1:n.341G>T
XM_011529060.2:c.205G>T XP_011527362.1:p.Glu69Ter
XM_011529061.2:c.151G>T XP_011527363.1:p.Glu51Ter
XM_011529062.2:c.205G>T XP_011527364.1:p.Glu69Ter
XM_011529063.2:c.205G>T XP_011527365.1:p.Glu69Ter
XM_011529064.2:c.205G>T XP_011527366.1:p.Glu69Ter
XM_011529065.2:c.205G>T XP_011527367.1:p.Glu69Ter
XM_017028087.2:c.142G>T XP_016883576.1:p.Glu48Ter
XR_936641.2:n.328G>T
NM_030777.4:c.142G>T MANE Select NP_110404.1:p.Glu48Ter