Canonical Allele Identifier: CA1821104975

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133651A= , CM000670.2:g.133133651A=	GRCh38
NC_000008.10:g.134145895A= , CM000670.1:g.134145895A=	GRCh37
NC_000008.9:g.134215077A=	NCBI36
NG_015832.1:g.271691A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8179A= MANE Select	ENSP00000220616.4:p.Thr2727=
ENST00000220616.8:c.8179A=	ENSP00000220616.4:p.Thr2727=
ENST00000519178.5:c.3545A=
ENST00000519543.5:c.2578A=	ENSP00000430430.1:p.Thr860=
ENST00000521107.1:c.391A=	ENSP00000430161.1:p.Thr131=
ENST00000522691.1:n.265A=
ENST00000523756.5:c.4834A=
NM_003235.4:c.8179A=	NP_003226.4:p.Thr2727=
XM_005251038.3:c.7987A=	XP_005251095.1:p.Thr2663=
XM_006716622.2:c.8116A=	XP_006716685.1:p.Thr2706=
XM_005251038.4:c.7987A=	XP_005251095.1:p.Thr2663=
XM_006716622.3:c.8116A=	XP_006716685.1:p.Thr2706=
XM_017013793.1:c.8113A=	XP_016869282.1:p.Thr2705=
XM_017013794.1:c.8044A=	XP_016869283.1:p.Thr2682=
XM_017013795.1:c.8008A=	XP_016869284.1:p.Thr2670=
XM_017013796.1:c.7960A=	XP_016869285.1:p.Thr2654=
XM_017013797.1:c.7918A=	XP_016869286.1:p.Thr2640=
NM_003235.5:c.8179A= MANE Select	NP_003226.4:p.Thr2727=