Canonical Allele Identifier: CA2653171902

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46726747-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726747A>T , CM000682.2:g.46726747A>T	GRCh38
NC_000020.10:g.45355386A>T , CM000682.1:g.45355386A>T	GRCh37
NC_000020.9:g.44788793A>T	NCBI36
NG_016284.1:g.22108A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-117A>T MANE Select	ENSP00000352216.2:n.1289-117A>T
ENST00000359271.3:c.1289-117A>T	ENSP00000352216.2:n.1289-117A>T
NM_030777.3:c.1289-117A>T	NP_110404.1:n.1289-117A>T
XM_011529060.1:c.1352-117A>T	XP_011527362.1:n.1352-117A>T
XM_011529061.1:c.1298-117A>T	XP_011527363.1:n.1298-117A>T
XM_011529062.1:c.1352-68A>T	XP_011527364.1:n.1352-68A>T
XM_011529063.1:c.1352-117A>T	XP_011527365.1:n.1352-117A>T
XM_011529064.1:c.1352-68A>T	XP_011527366.1:n.1352-68A>T
XM_011529065.1:c.1352-117A>T	XP_011527367.1:n.1352-117A>T
XR_936641.1:n.1488-68A>T
XM_011529060.2:c.1352-117A>T	XP_011527362.1:n.1352-117A>T
XM_011529061.2:c.1298-117A>T	XP_011527363.1:n.1298-117A>T
XM_011529062.2:c.1352-68A>T	XP_011527364.1:n.1352-68A>T
XM_011529063.2:c.1352-117A>T	XP_011527365.1:n.1352-117A>T
XM_011529064.2:c.1352-68A>T	XP_011527366.1:n.1352-68A>T
XM_011529065.2:c.1352-117A>T	XP_011527367.1:n.1352-117A>T
XM_017028087.2:c.1289-117A>T	XP_016883576.1:n.1289-117A>T
XR_936641.2:n.1475-68A>T
NM_030777.4:c.1289-117A>T MANE Select	NP_110404.1:n.1289-117A>T