Canonical Allele Identifier: CA1821104934

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133563C= , CM000670.2:g.133133563C=	GRCh38
NC_000008.10:g.134145807C= , CM000670.1:g.134145807C=	GRCh37
NC_000008.9:g.134214989C=	NCBI36
NG_015832.1:g.271603C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8091C= MANE Select	ENSP00000220616.4:p.Tyr2697=
ENST00000220616.8:c.8091C=	ENSP00000220616.4:p.Tyr2697=
ENST00000519178.5:c.3457C=
ENST00000519543.5:c.2490C=	ENSP00000430430.1:p.Tyr830=
ENST00000521107.1:c.303C=	ENSP00000430161.1:p.Tyr101=
ENST00000522691.1:n.177C=
ENST00000523756.5:c.4746C=
NM_003235.4:c.8091C=	NP_003226.4:p.Tyr2697=
XM_005251038.3:c.7899C=	XP_005251095.1:p.Tyr2633=
XM_006716622.2:c.8028C=	XP_006716685.1:p.Tyr2676=
XM_005251038.4:c.7899C=	XP_005251095.1:p.Tyr2633=
XM_006716622.3:c.8028C=	XP_006716685.1:p.Tyr2676=
XM_017013793.1:c.8025C=	XP_016869282.1:p.Tyr2675=
XM_017013794.1:c.7956C=	XP_016869283.1:p.Tyr2652=
XM_017013795.1:c.7920C=	XP_016869284.1:p.Tyr2640=
XM_017013796.1:c.7872C=	XP_016869285.1:p.Tyr2624=
XM_017013797.1:c.7830C=	XP_016869286.1:p.Tyr2610=
NM_003235.5:c.8091C= MANE Select	NP_003226.4:p.Tyr2697=