Canonical Allele Identifier: CA1821104921

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133543C= , CM000670.2:g.133133543C=	GRCh38
NC_000008.10:g.134145787C= , CM000670.1:g.134145787C=	GRCh37
NC_000008.9:g.134214969C=	NCBI36
NG_015832.1:g.271583C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8071C= MANE Select	ENSP00000220616.4:p.Arg2691=
ENST00000220616.8:c.8071C=	ENSP00000220616.4:p.Arg2691=
ENST00000519178.5:c.3437C=
ENST00000519543.5:c.2470C=	ENSP00000430430.1:p.Arg824=
ENST00000521107.1:c.283C=	ENSP00000430161.1:p.Arg95=
ENST00000522691.1:n.157C=
ENST00000523756.5:c.4726C=
NM_003235.4:c.8071C=	NP_003226.4:p.Arg2691=
XM_005251038.3:c.7879C=	XP_005251095.1:p.Arg2627=
XM_006716622.2:c.8008C=	XP_006716685.1:p.Arg2670=
XM_005251038.4:c.7879C=	XP_005251095.1:p.Arg2627=
XM_006716622.3:c.8008C=	XP_006716685.1:p.Arg2670=
XM_017013793.1:c.8005C=	XP_016869282.1:p.Arg2669=
XM_017013794.1:c.7936C=	XP_016869283.1:p.Arg2646=
XM_017013795.1:c.7900C=	XP_016869284.1:p.Arg2634=
XM_017013796.1:c.7852C=	XP_016869285.1:p.Arg2618=
XM_017013797.1:c.7810C=	XP_016869286.1:p.Arg2604=
NM_003235.5:c.8071C= MANE Select	NP_003226.4:p.Arg2691=