Canonical Allele Identifier: CA1821050315

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133022121G= , CM000670.2:g.133022121G=	GRCh38
NC_000008.10:g.134034366G= , CM000670.1:g.134034366G=	GRCh37
NC_000008.9:g.134103548G=	NCBI36
NG_015832.1:g.160162G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003235.5:c.7007G= MANE Select	NP_003226.4:p.Arg2336=
ENST00000220616.9:c.7007G= MANE Select	ENSP00000220616.4:p.Arg2336=
NM_003235.4:c.7007G=	NP_003226.4:p.Arg2336=
ENST00000220616.8:c.7007G=	ENSP00000220616.4:p.Arg2336=
ENST00000518108.1:c.393G=
ENST00000519178.5:c.2373G=
ENST00000519543.5:c.1406G=	ENSP00000430430.1:p.Arg469=
ENST00000523756.5:c.3662G=
XM_005251038.3:c.6815G=	XP_005251095.1:p.Arg2272=
XM_005251038.4:c.6815G=	XP_005251095.1:p.Arg2272=
XM_006716622.2:c.6944G=	XP_006716685.1:p.Arg2315=
XM_006716622.3:c.6944G=	XP_006716685.1:p.Arg2315=
XM_017013793.1:c.6941G=	XP_016869282.1:p.Arg2314=
XM_017013794.1:c.7007G=	XP_016869283.1:p.Arg2336=
XM_017013795.1:c.6836G=	XP_016869284.1:p.Arg2279=
XM_017013796.1:c.6788G=	XP_016869285.1:p.Arg2263=
XM_017013797.1:c.6746G=	XP_016869286.1:p.Arg2249=
XM_017013798.1:c.7007G=	XP_016869287.1:p.Arg2336=