Canonical Allele Identifier: CA2366796912

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726919C= , CM000682.2:g.46726919C=	GRCh38
NC_000020.10:g.45355558C= , CM000682.1:g.45355558C=	GRCh37
NC_000020.9:g.44788965C=	NCBI36
NG_016284.1:g.22280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1344C= MANE Select	ENSP00000352216.2:p.Phe448=
ENST00000359271.3:c.1344C=	ENSP00000352216.2:p.Phe448=
NM_030777.3:c.1344C=	NP_110404.1:p.Phe448=
XM_011529060.1:c.1407C=	XP_011527362.1:p.Phe469=
XM_011529061.1:c.1353C=	XP_011527363.1:p.Phe451=
XM_011529062.1:c.1456C=	XP_011527364.1:p.Arg486=
XM_011529063.1:c.1407C=	XP_011527365.1:p.Phe469=
XM_011529064.1:c.1456C=	XP_011527366.1:p.Arg486=
XM_011529065.1:c.1407C=	XP_011527367.1:p.Phe469=
XR_936641.1:n.1592C=
XM_011529060.2:c.1407C=	XP_011527362.1:p.Phe469=
XM_011529061.2:c.1353C=	XP_011527363.1:p.Phe451=
XM_011529062.2:c.1456C=	XP_011527364.1:p.Arg486=
XM_011529063.2:c.1407C=	XP_011527365.1:p.Phe469=
XM_011529064.2:c.1456C=	XP_011527366.1:p.Arg486=
XM_011529065.2:c.1407C=	XP_011527367.1:p.Phe469=
XM_017028087.2:c.1344C=	XP_016883576.1:p.Phe448=
XR_936641.2:n.1579C=
NM_030777.4:c.1344C= MANE Select	NP_110404.1:p.Phe448=