Canonical Allele Identifier: CA2366796163

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725360T= , CM000682.2:g.46725360T=	GRCh38
NC_000020.10:g.45353999T= , CM000682.1:g.45353999T=	GRCh37
NC_000020.9:g.44787406T=	NCBI36
NG_016284.1:g.20721T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.324T= MANE Select	ENSP00000352216.2:p.Val108=
ENST00000359271.3:c.324T=	ENSP00000352216.2:p.Val108=
ENST00000611837.1:n.476T=
NM_030777.3:c.324T=	NP_110404.1:p.Val108=
XM_011529060.1:c.387T=	XP_011527362.1:p.Val129=
XM_011529061.1:c.333T=	XP_011527363.1:p.Val111=
XM_011529062.1:c.387T=	XP_011527364.1:p.Val129=
XM_011529063.1:c.387T=	XP_011527365.1:p.Val129=
XM_011529064.1:c.387T=	XP_011527366.1:p.Val129=
XM_011529065.1:c.387T=	XP_011527367.1:p.Val129=
XR_936641.1:n.523T=
XM_011529060.2:c.387T=	XP_011527362.1:p.Val129=
XM_011529061.2:c.333T=	XP_011527363.1:p.Val111=
XM_011529062.2:c.387T=	XP_011527364.1:p.Val129=
XM_011529063.2:c.387T=	XP_011527365.1:p.Val129=
XM_011529064.2:c.387T=	XP_011527366.1:p.Val129=
XM_011529065.2:c.387T=	XP_011527367.1:p.Val129=
XM_017028087.2:c.324T=	XP_016883576.1:p.Val108=
XR_936641.2:n.510T=
NM_030777.4:c.324T= MANE Select	NP_110404.1:p.Val108=