Canonical Allele Identifier: CA2366796878

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726864T= , CM000682.2:g.46726864T=	GRCh38
NC_000020.10:g.45355503T= , CM000682.1:g.45355503T=	GRCh37
NC_000020.9:g.44788910T=	NCBI36
NG_016284.1:g.22225T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289T= MANE Select	ENSP00000352216.2:p.Val430=
ENST00000359271.3:c.1289T=	ENSP00000352216.2:p.Val430=
NM_030777.3:c.1289T=	NP_110404.1:p.Val430=
XM_011529060.1:c.1352T=	XP_011527362.1:p.Val451=
XM_011529061.1:c.1298T=	XP_011527363.1:p.Val433=
XM_011529062.1:c.1401T=	XP_011527364.1:p.Ser467=
XM_011529063.1:c.1352T=	XP_011527365.1:p.Val451=
XM_011529064.1:c.1401T=	XP_011527366.1:p.Ser467=
XM_011529065.1:c.1352T=	XP_011527367.1:p.Val451=
XR_936641.1:n.1537T=
XM_011529060.2:c.1352T=	XP_011527362.1:p.Val451=
XM_011529061.2:c.1298T=	XP_011527363.1:p.Val433=
XM_011529062.2:c.1401T=	XP_011527364.1:p.Ser467=
XM_011529063.2:c.1352T=	XP_011527365.1:p.Val451=
XM_011529064.2:c.1401T=	XP_011527366.1:p.Ser467=
XM_011529065.2:c.1352T=	XP_011527367.1:p.Val451=
XM_017028087.2:c.1289T=	XP_016883576.1:p.Val430=
XR_936641.2:n.1524T=
NM_030777.4:c.1289T= MANE Select	NP_110404.1:p.Val430=