Canonical Allele Identifier: CA2366796220

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725469G= , CM000682.2:g.46725469G=	GRCh38
NC_000020.10:g.45354108G= , CM000682.1:g.45354108G=	GRCh37
NC_000020.9:g.44787515G=	NCBI36
NG_016284.1:g.20830G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.433G= MANE Select	ENSP00000352216.2:p.Val145=
ENST00000359271.3:c.433G=	ENSP00000352216.2:p.Val145=
ENST00000611837.1:n.585G=
NM_030777.3:c.433G=	NP_110404.1:p.Val145=
XM_011529060.1:c.496G=	XP_011527362.1:p.Val166=
XM_011529061.1:c.442G=	XP_011527363.1:p.Val148=
XM_011529062.1:c.496G=	XP_011527364.1:p.Val166=
XM_011529063.1:c.496G=	XP_011527365.1:p.Val166=
XM_011529064.1:c.496G=	XP_011527366.1:p.Val166=
XM_011529065.1:c.496G=	XP_011527367.1:p.Val166=
XR_936641.1:n.632G=
XM_011529060.2:c.496G=	XP_011527362.1:p.Val166=
XM_011529061.2:c.442G=	XP_011527363.1:p.Val148=
XM_011529062.2:c.496G=	XP_011527364.1:p.Val166=
XM_011529063.2:c.496G=	XP_011527365.1:p.Val166=
XM_011529064.2:c.496G=	XP_011527366.1:p.Val166=
XM_011529065.2:c.496G=	XP_011527367.1:p.Val166=
XM_017028087.2:c.433G=	XP_016883576.1:p.Val145=
XR_936641.2:n.619G=
NM_030777.4:c.433G= MANE Select	NP_110404.1:p.Val145=