Canonical Allele Identifier: CA1821041058

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133012017C= , CM000670.2:g.133012017C=	GRCh38
NC_000008.10:g.134024262C= , CM000670.1:g.134024262C=	GRCh37
NC_000008.9:g.134093444C=	NCBI36
NG_015832.1:g.150058C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003235.5:c.6379C= MANE Select	NP_003226.4:p.Arg2127=
ENST00000220616.9:c.6379C= MANE Select	ENSP00000220616.4:p.Arg2127=
NM_003235.4:c.6379C=	NP_003226.4:p.Arg2127=
ENST00000220616.8:c.6379C=	ENSP00000220616.4:p.Arg2127=
ENST00000519178.5:c.1745C=
ENST00000519543.5:c.778C=	ENSP00000430430.1:p.Arg260=
ENST00000522523.5:n.440C=
ENST00000522797.1:c.379C=
ENST00000523756.5:c.3034C=
XM_005251038.3:c.6187C=	XP_005251095.1:p.Arg2063=
XM_005251038.4:c.6187C=	XP_005251095.1:p.Arg2063=
XM_006716622.2:c.6316C=	XP_006716685.1:p.Arg2106=
XM_006716622.3:c.6316C=	XP_006716685.1:p.Arg2106=
XM_017013793.1:c.6313C=	XP_016869282.1:p.Arg2105=
XM_017013794.1:c.6379C=	XP_016869283.1:p.Arg2127=
XM_017013795.1:c.6208C=	XP_016869284.1:p.Arg2070=
XM_017013796.1:c.6160C=	XP_016869285.1:p.Arg2054=
XM_017013797.1:c.6118C=	XP_016869286.1:p.Arg2040=
XM_017013798.1:c.6379C=	XP_016869287.1:p.Arg2127=