Canonical Allele Identifier: CA1821104964

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133631A= , CM000670.2:g.133133631A=	GRCh38
NC_000008.10:g.134145875A= , CM000670.1:g.134145875A=	GRCh37
NC_000008.9:g.134215057A=	NCBI36
NG_015832.1:g.271671A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8159A= MANE Select	ENSP00000220616.4:p.Lys2720=
ENST00000220616.8:c.8159A=	ENSP00000220616.4:p.Lys2720=
ENST00000519178.5:c.3525A=
ENST00000519543.5:c.2558A=	ENSP00000430430.1:p.Lys853=
ENST00000521107.1:c.371A=	ENSP00000430161.1:p.Lys124=
ENST00000522691.1:n.245A=
ENST00000523756.5:c.4814A=
NM_003235.4:c.8159A=	NP_003226.4:p.Lys2720=
XM_005251038.3:c.7967A=	XP_005251095.1:p.Lys2656=
XM_006716622.2:c.8096A=	XP_006716685.1:p.Lys2699=
XM_005251038.4:c.7967A=	XP_005251095.1:p.Lys2656=
XM_006716622.3:c.8096A=	XP_006716685.1:p.Lys2699=
XM_017013793.1:c.8093A=	XP_016869282.1:p.Lys2698=
XM_017013794.1:c.8024A=	XP_016869283.1:p.Lys2675=
XM_017013795.1:c.7988A=	XP_016869284.1:p.Lys2663=
XM_017013796.1:c.7940A=	XP_016869285.1:p.Lys2647=
XM_017013797.1:c.7898A=	XP_016869286.1:p.Lys2633=
NM_003235.5:c.8159A= MANE Select	NP_003226.4:p.Lys2720=