Canonical Allele Identifier: CA2366796070
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725183C= , CM000682.2:g.46725183C= GRCh38
NC_000020.10:g.45353822C= , CM000682.1:g.45353822C= GRCh37
NC_000020.9:g.44787229C= NCBI36
NG_016284.1:g.20544C=

Transcript Alleles

HGVS Amino-acid change
ENST00000359271.4:c.147C= MANE Select ENSP00000352216.2:p.Phe49=
ENST00000359271.3:c.147C= ENSP00000352216.2:p.Phe49=
ENST00000611837.1:n.299C=
NM_030777.3:c.147C= NP_110404.1:p.Phe49=
XM_011529060.1:c.210C= XP_011527362.1:p.Phe70=
XM_011529061.1:c.156C= XP_011527363.1:p.Phe52=
XM_011529062.1:c.210C= XP_011527364.1:p.Phe70=
XM_011529063.1:c.210C= XP_011527365.1:p.Phe70=
XM_011529064.1:c.210C= XP_011527366.1:p.Phe70=
XM_011529065.1:c.210C= XP_011527367.1:p.Phe70=
XR_936641.1:n.346C=
XM_011529060.2:c.210C= XP_011527362.1:p.Phe70=
XM_011529061.2:c.156C= XP_011527363.1:p.Phe52=
XM_011529062.2:c.210C= XP_011527364.1:p.Phe70=
XM_011529063.2:c.210C= XP_011527365.1:p.Phe70=
XM_011529064.2:c.210C= XP_011527366.1:p.Phe70=
XM_011529065.2:c.210C= XP_011527367.1:p.Phe70=
XM_017028087.2:c.147C= XP_016883576.1:p.Phe49=
XR_936641.2:n.333C=
NM_030777.4:c.147C= MANE Select NP_110404.1:p.Phe49=