Canonical Allele Identifier: CA409271591

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726862A>G , CM000682.2:g.46726862A>G	GRCh38
NC_000020.10:g.45355501A>G , CM000682.1:g.45355501A>G	GRCh37
NC_000020.9:g.44788908A>G	NCBI36
NG_016284.1:g.22223A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_030777.4:c.1289-2A>G MANE Select	NP_110404.1:n.1289-2A>G
ENST00000359271.4:c.1289-2A>G MANE Select	ENSP00000352216.2:n.1289-2A>G
NM_030777.3:c.1289-2A>G	NP_110404.1:n.1289-2A>G
ENST00000359271.3:c.1289-2A>G	ENSP00000352216.2:n.1289-2A>G
XM_011529060.1:c.1352-2A>G	XP_011527362.1:n.1352-2A>G
XM_011529060.2:c.1352-2A>G	XP_011527362.1:n.1352-2A>G
XM_011529061.1:c.1298-2A>G	XP_011527363.1:n.1298-2A>G
XM_011529061.2:c.1298-2A>G	XP_011527363.1:n.1298-2A>G
XM_011529062.1:c.1399A>G	XP_011527364.1:p.Ser467Gly
XM_011529062.2:c.1399A>G	XP_011527364.1:p.Ser467Gly
XM_011529063.1:c.1352-2A>G	XP_011527365.1:n.1352-2A>G
XM_011529063.2:c.1352-2A>G	XP_011527365.1:n.1352-2A>G
XM_011529064.1:c.1399A>G	XP_011527366.1:p.Ser467Gly
XM_011529064.2:c.1399A>G	XP_011527366.1:p.Ser467Gly
XM_011529065.1:c.1352-2A>G	XP_011527367.1:n.1352-2A>G
XM_011529065.2:c.1352-2A>G	XP_011527367.1:n.1352-2A>G
XM_017028087.2:c.1289-2A>G	XP_016883576.1:n.1289-2A>G
XR_936641.1:n.1535A>G
XR_936641.2:n.1522A>G