Canonical Allele Identifier: CA2366796842
Gene: SLC2A10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726786A= , CM000682.2:g.46726786A= GRCh38
NC_000020.10:g.45355425A= , CM000682.1:g.45355425A= GRCh37
NC_000020.9:g.44788832A= NCBI36
NG_016284.1:g.22147A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1289-78A= MANE Select ENSP00000352216.2:n.1289-78A=
ENST00000359271.3:c.1289-78A= ENSP00000352216.2:n.1289-78A=
NM_030777.3:c.1289-78A= NP_110404.1:n.1289-78A=
XM_011529060.1:c.1352-78A= XP_011527362.1:n.1352-78A=
XM_011529061.1:c.1298-78A= XP_011527363.1:n.1298-78A=
XM_011529062.1:c.1352-29A= XP_011527364.1:n.1352-29A=
XM_011529063.1:c.1352-78A= XP_011527365.1:n.1352-78A=
XM_011529064.1:c.1352-29A= XP_011527366.1:n.1352-29A=
XM_011529065.1:c.1352-78A= XP_011527367.1:n.1352-78A=
XR_936641.1:n.1488-29A=
XM_011529060.2:c.1352-78A= XP_011527362.1:n.1352-78A=
XM_011529061.2:c.1298-78A= XP_011527363.1:n.1298-78A=
XM_011529062.2:c.1352-29A= XP_011527364.1:n.1352-29A=
XM_011529063.2:c.1352-78A= XP_011527365.1:n.1352-78A=
XM_011529064.2:c.1352-29A= XP_011527366.1:n.1352-29A=
XM_011529065.2:c.1352-78A= XP_011527367.1:n.1352-78A=
XM_017028087.2:c.1289-78A= XP_016883576.1:n.1289-78A=
XR_936641.2:n.1475-29A=
NM_030777.4:c.1289-78A= MANE Select NP_110404.1:n.1289-78A=