Canonical Allele Identifier: CA2366795944
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46724916T= , CM000682.2:g.46724916T= GRCh38
NC_000020.10:g.45353555T= , CM000682.1:g.45353555T= GRCh37
NC_000020.9:g.44786962T= NCBI36
NG_016284.1:g.20277T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.5-125T= MANE Select ENSP00000352216.2:n.5-125T=
ENST00000359271.3:c.5-125T= ENSP00000352216.2:n.5-125T=
ENST00000611837.1:n.157-125T=
NM_030777.3:c.5-125T= NP_110404.1:n.5-125T=
XM_011529060.1:c.68-125T= XP_011527362.1:n.68-125T=
XM_011529061.1:c.14-125T= XP_011527363.1:n.14-125T=
XM_011529062.1:c.68-125T= XP_011527364.1:n.68-125T=
XM_011529063.1:c.68-125T= XP_011527365.1:n.68-125T=
XM_011529064.1:c.68-125T= XP_011527366.1:n.68-125T=
XM_011529065.1:c.68-125T= XP_011527367.1:n.68-125T=
XR_936641.1:n.204-125T=
XM_011529060.2:c.68-125T= XP_011527362.1:n.68-125T=
XM_011529061.2:c.14-125T= XP_011527363.1:n.14-125T=
XM_011529062.2:c.68-125T= XP_011527364.1:n.68-125T=
XM_011529063.2:c.68-125T= XP_011527365.1:n.68-125T=
XM_011529064.2:c.68-125T= XP_011527366.1:n.68-125T=
XM_011529065.2:c.68-125T= XP_011527367.1:n.68-125T=
XM_017028087.2:c.5-125T= XP_016883576.1:n.5-125T=
XR_936641.2:n.191-125T=
NM_030777.4:c.5-125T= MANE Select NP_110404.1:n.5-125T=