Canonical Allele Identifier: CA2653171912

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46726765-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726765C>A , CM000682.2:g.46726765C>A	GRCh38
NC_000020.10:g.45355404C>A , CM000682.1:g.45355404C>A	GRCh37
NC_000020.9:g.44788811C>A	NCBI36
NG_016284.1:g.22126C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-99C>A MANE Select	ENSP00000352216.2:n.1289-99C>A
ENST00000359271.3:c.1289-99C>A	ENSP00000352216.2:n.1289-99C>A
NM_030777.3:c.1289-99C>A	NP_110404.1:n.1289-99C>A
XM_011529060.1:c.1352-99C>A	XP_011527362.1:n.1352-99C>A
XM_011529061.1:c.1298-99C>A	XP_011527363.1:n.1298-99C>A
XM_011529062.1:c.1352-50C>A	XP_011527364.1:n.1352-50C>A
XM_011529063.1:c.1352-99C>A	XP_011527365.1:n.1352-99C>A
XM_011529064.1:c.1352-50C>A	XP_011527366.1:n.1352-50C>A
XM_011529065.1:c.1352-99C>A	XP_011527367.1:n.1352-99C>A
XR_936641.1:n.1488-50C>A
XM_011529060.2:c.1352-99C>A	XP_011527362.1:n.1352-99C>A
XM_011529061.2:c.1298-99C>A	XP_011527363.1:n.1298-99C>A
XM_011529062.2:c.1352-50C>A	XP_011527364.1:n.1352-50C>A
XM_011529063.2:c.1352-99C>A	XP_011527365.1:n.1352-99C>A
XM_011529064.2:c.1352-50C>A	XP_011527366.1:n.1352-50C>A
XM_011529065.2:c.1352-99C>A	XP_011527367.1:n.1352-99C>A
XM_017028087.2:c.1289-99C>A	XP_016883576.1:n.1289-99C>A
XR_936641.2:n.1475-50C>A
NM_030777.4:c.1289-99C>A MANE Select	NP_110404.1:n.1289-99C>A