Canonical Allele Identifier: CA2366796278

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725611C= , CM000682.2:g.46725611C=	GRCh38
NC_000020.10:g.45354250C= , CM000682.1:g.45354250C=	GRCh37
NC_000020.9:g.44787657C=	NCBI36
NG_016284.1:g.20972C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.575C= MANE Select	ENSP00000352216.2:p.Thr192=
ENST00000359271.3:c.575C=	ENSP00000352216.2:p.Thr192=
NM_030777.3:c.575C=	NP_110404.1:p.Thr192=
XM_011529060.1:c.638C=	XP_011527362.1:p.Thr213=
XM_011529061.1:c.584C=	XP_011527363.1:p.Thr195=
XM_011529062.1:c.638C=	XP_011527364.1:p.Thr213=
XM_011529063.1:c.638C=	XP_011527365.1:p.Thr213=
XM_011529064.1:c.638C=	XP_011527366.1:p.Thr213=
XM_011529065.1:c.638C=	XP_011527367.1:p.Thr213=
XR_936641.1:n.774C=
XM_011529060.2:c.638C=	XP_011527362.1:p.Thr213=
XM_011529061.2:c.584C=	XP_011527363.1:p.Thr195=
XM_011529062.2:c.638C=	XP_011527364.1:p.Thr213=
XM_011529063.2:c.638C=	XP_011527365.1:p.Thr213=
XM_011529064.2:c.638C=	XP_011527366.1:p.Thr213=
XM_011529065.2:c.638C=	XP_011527367.1:p.Thr213=
XM_017028087.2:c.575C=	XP_016883576.1:p.Thr192=
XR_936641.2:n.761C=
NM_030777.4:c.575C= MANE Select	NP_110404.1:p.Thr192=