Canonical Allele Identifier: CA1821046397

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017940G= , CM000670.2:g.133017940G=	GRCh38
NC_000008.10:g.134030185G= , CM000670.1:g.134030185G=	GRCh37
NC_000008.9:g.134099367G=	NCBI36
NG_015832.1:g.155981G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003235.5:c.6725G= MANE Select	NP_003226.4:p.Arg2242=
ENST00000220616.9:c.6725G= MANE Select	ENSP00000220616.4:p.Arg2242=
NM_003235.4:c.6725G=	NP_003226.4:p.Arg2242=
ENST00000220616.8:c.6725G=	ENSP00000220616.4:p.Arg2242=
ENST00000518108.1:c.168+74G=
ENST00000519178.5:c.2091G=
ENST00000519543.5:c.1124G=	ENSP00000430430.1:p.Arg375=
ENST00000522523.5:n.786G=
ENST00000523756.5:c.3380G=
XM_005251038.3:c.6533G=	XP_005251095.1:p.Arg2178=
XM_005251038.4:c.6533G=	XP_005251095.1:p.Arg2178=
XM_006716622.2:c.6662G=	XP_006716685.1:p.Arg2221=
XM_006716622.3:c.6662G=	XP_006716685.1:p.Arg2221=
XM_017013793.1:c.6659G=	XP_016869282.1:p.Arg2220=
XM_017013794.1:c.6725G=	XP_016869283.1:p.Arg2242=
XM_017013795.1:c.6554G=	XP_016869284.1:p.Arg2185=
XM_017013796.1:c.6506G=	XP_016869285.1:p.Arg2169=
XM_017013797.1:c.6464G=	XP_016869286.1:p.Arg2155=
XM_017013798.1:c.6725G=	XP_016869287.1:p.Arg2242=