Canonical Allele Identifier: CA1821005038

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971811G= , CM000670.2:g.132971811G=	GRCh38
NC_000008.10:g.133984056G= , CM000670.1:g.133984056G=	GRCh37
NC_000008.9:g.134053238G=	NCBI36
NG_015832.1:g.109852G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5993G= MANE Select	ENSP00000220616.4:p.Arg1998=
ENST00000220616.8:c.5993G=	ENSP00000220616.4:p.Arg1998=
ENST00000519178.5:c.1359G=
ENST00000519543.5:c.455G=	ENSP00000430430.1:p.Arg152=
ENST00000520089.5:n.102G=
ENST00000520197.5:n.130G=
ENST00000523756.5:c.2648G=
NM_003235.4:c.5993G=	NP_003226.4:p.Arg1998=
XM_005251038.3:c.5801G=	XP_005251095.1:p.Arg1934=
XM_005251040.3:c.5993G=	XP_005251097.1:p.Arg1998=
XM_005251042.3:c.5993G=	XP_005251099.1:p.Arg1998=
XM_005251043.3:c.5993G=	XP_005251100.1:p.Arg1998=
XM_006716622.2:c.5993G=	XP_006716685.1:p.Arg1998=
XM_005251038.4:c.5801G=	XP_005251095.1:p.Arg1934=
XM_005251040.4:c.5993G=	XP_005251097.1:p.Arg1998=
XM_005251042.4:c.5993G=	XP_005251099.1:p.Arg1998=
XM_006716622.3:c.5993G=	XP_006716685.1:p.Arg1998=
XM_017013793.1:c.5927G=	XP_016869282.1:p.Arg1976=
XM_017013794.1:c.5993G=	XP_016869283.1:p.Arg1998=
XM_017013795.1:c.5822G=	XP_016869284.1:p.Arg1941=
XM_017013796.1:c.5774G=	XP_016869285.1:p.Arg1925=
XM_017013797.1:c.5732G=	XP_016869286.1:p.Arg1911=
XM_017013798.1:c.5993G=	XP_016869287.1:p.Arg1998=
XM_017013799.1:c.5993G=	XP_016869288.1:p.Arg1998=
XM_017013800.1:c.5993G=	XP_016869289.1:p.Arg1998=
NM_003235.5:c.5993G= MANE Select	NP_003226.4:p.Arg1998=