Canonical Allele Identifier: CA1821005061

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971836C= , CM000670.2:g.132971836C=	GRCh38
NC_000008.10:g.133984081C= , CM000670.1:g.133984081C=	GRCh37
NC_000008.9:g.134053263C=	NCBI36
NG_015832.1:g.109877C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6018C= MANE Select	ENSP00000220616.4:p.Cys2006=
ENST00000220616.8:c.6018C=	ENSP00000220616.4:p.Cys2006=
ENST00000519178.5:c.1384C=
ENST00000519294.5:n.10C=
ENST00000519543.5:c.480C=	ENSP00000430430.1:p.Cys160=
ENST00000520089.5:n.127C=
ENST00000520197.5:n.155C=
ENST00000523756.5:c.2673C=
NM_003235.4:c.6018C=	NP_003226.4:p.Cys2006=
XM_005251038.3:c.5826C=	XP_005251095.1:p.Cys1942=
XM_005251040.3:c.6018C=	XP_005251097.1:p.Cys2006=
XM_005251042.3:c.6018C=	XP_005251099.1:p.Cys2006=
XM_005251043.3:c.6018C=	XP_005251100.1:p.Cys2006=
XM_006716622.2:c.6018C=	XP_006716685.1:p.Cys2006=
XM_005251038.4:c.5826C=	XP_005251095.1:p.Cys1942=
XM_005251040.4:c.6018C=	XP_005251097.1:p.Cys2006=
XM_005251042.4:c.6018C=	XP_005251099.1:p.Cys2006=
XM_006716622.3:c.6018C=	XP_006716685.1:p.Cys2006=
XM_017013793.1:c.5952C=	XP_016869282.1:p.Cys1984=
XM_017013794.1:c.6018C=	XP_016869283.1:p.Cys2006=
XM_017013795.1:c.5847C=	XP_016869284.1:p.Cys1949=
XM_017013796.1:c.5799C=	XP_016869285.1:p.Cys1933=
XM_017013797.1:c.5757C=	XP_016869286.1:p.Cys1919=
XM_017013798.1:c.6018C=	XP_016869287.1:p.Cys2006=
XM_017013799.1:c.6018C=	XP_016869288.1:p.Cys2006=
XM_017013800.1:c.6018C=	XP_016869289.1:p.Cys2006=
NM_003235.5:c.6018C= MANE Select	NP_003226.4:p.Cys2006=