Canonical Allele Identifier: CA1821104938

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133572C= , CM000670.2:g.133133572C=	GRCh38
NC_000008.10:g.134145816C= , CM000670.1:g.134145816C=	GRCh37
NC_000008.9:g.134214998C=	NCBI36
NG_015832.1:g.271612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8100C= MANE Select	ENSP00000220616.4:p.Phe2700=
ENST00000220616.8:c.8100C=	ENSP00000220616.4:p.Phe2700=
ENST00000519178.5:c.3466C=
ENST00000519543.5:c.2499C=	ENSP00000430430.1:p.Phe833=
ENST00000521107.1:c.312C=	ENSP00000430161.1:p.Phe104=
ENST00000522691.1:n.186C=
ENST00000523756.5:c.4755C=
NM_003235.4:c.8100C=	NP_003226.4:p.Phe2700=
XM_005251038.3:c.7908C=	XP_005251095.1:p.Phe2636=
XM_006716622.2:c.8037C=	XP_006716685.1:p.Phe2679=
XM_005251038.4:c.7908C=	XP_005251095.1:p.Phe2636=
XM_006716622.3:c.8037C=	XP_006716685.1:p.Phe2679=
XM_017013793.1:c.8034C=	XP_016869282.1:p.Phe2678=
XM_017013794.1:c.7965C=	XP_016869283.1:p.Phe2655=
XM_017013795.1:c.7929C=	XP_016869284.1:p.Phe2643=
XM_017013796.1:c.7881C=	XP_016869285.1:p.Phe2627=
XM_017013797.1:c.7839C=	XP_016869286.1:p.Phe2613=
NM_003235.5:c.8100C= MANE Select	NP_003226.4:p.Phe2700=