Canonical Allele Identifier: CA1821104979

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133658C= , CM000670.2:g.133133658C=	GRCh38
NC_000008.10:g.134145902C= , CM000670.1:g.134145902C=	GRCh37
NC_000008.9:g.134215084C=	NCBI36
NG_015832.1:g.271698C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8186C= MANE Select	ENSP00000220616.4:p.Ala2729=
ENST00000220616.8:c.8186C=	ENSP00000220616.4:p.Ala2729=
ENST00000519178.5:c.3552C=
ENST00000519543.5:c.2585C=	ENSP00000430430.1:p.Ala862=
ENST00000521107.1:c.398C=	ENSP00000430161.1:p.Ala133=
ENST00000522691.1:n.272C=
ENST00000523756.5:c.4841C=
NM_003235.4:c.8186C=	NP_003226.4:p.Ala2729=
XM_005251038.3:c.7994C=	XP_005251095.1:p.Ala2665=
XM_006716622.2:c.8123C=	XP_006716685.1:p.Ala2708=
XM_005251038.4:c.7994C=	XP_005251095.1:p.Ala2665=
XM_006716622.3:c.8123C=	XP_006716685.1:p.Ala2708=
XM_017013793.1:c.8120C=	XP_016869282.1:p.Ala2707=
XM_017013794.1:c.8051C=	XP_016869283.1:p.Ala2684=
XM_017013795.1:c.8015C=	XP_016869284.1:p.Ala2672=
XM_017013796.1:c.7967C=	XP_016869285.1:p.Ala2656=
XM_017013797.1:c.7925C=	XP_016869286.1:p.Ala2642=
NM_003235.5:c.8186C= MANE Select	NP_003226.4:p.Ala2729=