Canonical Allele Identifier: CA2653171914

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46726768-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726768G>T , CM000682.2:g.46726768G>T	GRCh38
NC_000020.10:g.45355407G>T , CM000682.1:g.45355407G>T	GRCh37
NC_000020.9:g.44788814G>T	NCBI36
NG_016284.1:g.22129G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.1289-96G>T MANE Select	ENSP00000352216.2:n.1289-96G>T
ENST00000359271.3:c.1289-96G>T	ENSP00000352216.2:n.1289-96G>T
NM_030777.3:c.1289-96G>T	NP_110404.1:n.1289-96G>T
XM_011529060.1:c.1352-96G>T	XP_011527362.1:n.1352-96G>T
XM_011529061.1:c.1298-96G>T	XP_011527363.1:n.1298-96G>T
XM_011529062.1:c.1352-47G>T	XP_011527364.1:n.1352-47G>T
XM_011529063.1:c.1352-96G>T	XP_011527365.1:n.1352-96G>T
XM_011529064.1:c.1352-47G>T	XP_011527366.1:n.1352-47G>T
XM_011529065.1:c.1352-96G>T	XP_011527367.1:n.1352-96G>T
XR_936641.1:n.1488-47G>T
XM_011529060.2:c.1352-96G>T	XP_011527362.1:n.1352-96G>T
XM_011529061.2:c.1298-96G>T	XP_011527363.1:n.1298-96G>T
XM_011529062.2:c.1352-47G>T	XP_011527364.1:n.1352-47G>T
XM_011529063.2:c.1352-96G>T	XP_011527365.1:n.1352-96G>T
XM_011529064.2:c.1352-47G>T	XP_011527366.1:n.1352-47G>T
XM_011529065.2:c.1352-96G>T	XP_011527367.1:n.1352-96G>T
XM_017028087.2:c.1289-96G>T	XP_016883576.1:n.1289-96G>T
XR_936641.2:n.1475-47G>T
NM_030777.4:c.1289-96G>T MANE Select	NP_110404.1:n.1289-96G>T