Canonical Allele Identifier: CA293553

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726334G>A , CM000682.2:g.46726334G>A	GRCh38
NC_000020.10:g.45354973G>A , CM000682.1:g.45354973G>A	GRCh37
NC_000020.9:g.44788380G>A	NCBI36
NG_016284.1:g.21695G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1288+10G>A MANE Select	ENSP00000352216.2:n.1288+10G>A
ENST00000359271.3:c.1288+10G>A	ENSP00000352216.2:n.1288+10G>A
NM_030777.3:c.1288+10G>A	NP_110404.1:n.1288+10G>A
XM_011529060.1:c.1351+10G>A	XP_011527362.1:n.1351+10G>A
XM_011529061.1:c.1297+10G>A	XP_011527363.1:n.1297+10G>A
XM_011529062.1:c.1351+10G>A	XP_011527364.1:n.1351+10G>A
XM_011529063.1:c.1351+10G>A	XP_011527365.1:n.1351+10G>A
XM_011529064.1:c.1351+10G>A	XP_011527366.1:n.1351+10G>A
XM_011529065.1:c.1351+10G>A	XP_011527367.1:n.1351+10G>A
XR_936641.1:n.1487+10G>A
XM_011529060.2:c.1351+10G>A	XP_011527362.1:n.1351+10G>A
XM_011529061.2:c.1297+10G>A	XP_011527363.1:n.1297+10G>A
XM_011529062.2:c.1351+10G>A	XP_011527364.1:n.1351+10G>A
XM_011529063.2:c.1351+10G>A	XP_011527365.1:n.1351+10G>A
XM_011529064.2:c.1351+10G>A	XP_011527366.1:n.1351+10G>A
XM_011529065.2:c.1351+10G>A	XP_011527367.1:n.1351+10G>A
XM_017028087.2:c.1288+10G>A	XP_016883576.1:n.1288+10G>A
XR_936641.2:n.1474+10G>A
NM_030777.4:c.1288+10G>A MANE Select	NP_110404.1:n.1288+10G>A