Canonical Allele Identifier: CA2366796930

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726959A= , CM000682.2:g.46726959A=	GRCh38
NC_000020.10:g.45355598A= , CM000682.1:g.45355598A=	GRCh37
NC_000020.9:g.44789005A=	NCBI36
NG_016284.1:g.22320A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.1384A= MANE Select	ENSP00000352216.2:p.Ile462=
ENST00000359271.3:c.1384A=	ENSP00000352216.2:p.Ile462=
NM_030777.3:c.1384A=	NP_110404.1:p.Ile462=
XM_011529060.1:c.1447A=	XP_011527362.1:p.Ile483=
XM_011529061.1:c.1393A=	XP_011527363.1:p.Ile465=
XM_011529062.1:c.1496A=	XP_011527364.1:p.His499=
XM_011529063.1:c.1447A=	XP_011527365.1:p.Ile483=
XM_011529064.1:c.1496A=	XP_011527366.1:p.His499=
XM_011529065.1:c.1447A=	XP_011527367.1:p.Ile483=
XR_936641.1:n.1632A=
XM_011529060.2:c.1447A=	XP_011527362.1:p.Ile483=
XM_011529061.2:c.1393A=	XP_011527363.1:p.Ile465=
XM_011529062.2:c.1496A=	XP_011527364.1:p.His499=
XM_011529063.2:c.1447A=	XP_011527365.1:p.Ile483=
XM_011529064.2:c.1496A=	XP_011527366.1:p.His499=
XM_011529065.2:c.1447A=	XP_011527367.1:p.Ile483=
XM_017028087.2:c.1384A=	XP_016883576.1:p.Ile462=
XR_936641.2:n.1619A=
NM_030777.4:c.1384A= MANE Select	NP_110404.1:p.Ile462=