Canonical Allele Identifier: CA2366796865

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726839G= , CM000682.2:g.46726839G=	GRCh38
NC_000020.10:g.45355478G= , CM000682.1:g.45355478G=	GRCh37
NC_000020.9:g.44788885G=	NCBI36
NG_016284.1:g.22200G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-25G= MANE Select	ENSP00000352216.2:n.1289-25G=
ENST00000359271.3:c.1289-25G=	ENSP00000352216.2:n.1289-25G=
NM_030777.3:c.1289-25G=	NP_110404.1:n.1289-25G=
XM_011529060.1:c.1352-25G=	XP_011527362.1:n.1352-25G=
XM_011529061.1:c.1298-25G=	XP_011527363.1:n.1298-25G=
XM_011529062.1:c.1376G=	XP_011527364.1:p.Gly459=
XM_011529063.1:c.1352-25G=	XP_011527365.1:n.1352-25G=
XM_011529064.1:c.1376G=	XP_011527366.1:p.Gly459=
XM_011529065.1:c.1352-25G=	XP_011527367.1:n.1352-25G=
XR_936641.1:n.1512G=
XM_011529060.2:c.1352-25G=	XP_011527362.1:n.1352-25G=
XM_011529061.2:c.1298-25G=	XP_011527363.1:n.1298-25G=
XM_011529062.2:c.1376G=	XP_011527364.1:p.Gly459=
XM_011529063.2:c.1352-25G=	XP_011527365.1:n.1352-25G=
XM_011529064.2:c.1376G=	XP_011527366.1:p.Gly459=
XM_011529065.2:c.1352-25G=	XP_011527367.1:n.1352-25G=
XM_017028087.2:c.1289-25G=	XP_016883576.1:n.1289-25G=
XR_936641.2:n.1499G=
NM_030777.4:c.1289-25G= MANE Select	NP_110404.1:n.1289-25G=