Canonical Allele Identifier: CA1821104898

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133505T= , CM000670.2:g.133133505T=	GRCh38
NC_000008.10:g.134145749T= , CM000670.1:g.134145749T=	GRCh37
NC_000008.9:g.134214931T=	NCBI36
NG_015832.1:g.271545T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8033T= MANE Select	ENSP00000220616.4:p.Val2678=
ENST00000220616.8:c.8033T=	ENSP00000220616.4:p.Val2678=
ENST00000519178.5:c.3399T=
ENST00000519543.5:c.2432T=	ENSP00000430430.1:p.Val811=
ENST00000521107.1:c.245T=	ENSP00000430161.1:p.Val82=
ENST00000522691.1:n.119T=
ENST00000523756.5:c.4688T=
NM_003235.4:c.8033T=	NP_003226.4:p.Val2678=
XM_005251038.3:c.7841T=	XP_005251095.1:p.Val2614=
XM_006716622.2:c.7970T=	XP_006716685.1:p.Val2657=
XM_005251038.4:c.7841T=	XP_005251095.1:p.Val2614=
XM_006716622.3:c.7970T=	XP_006716685.1:p.Val2657=
XM_017013793.1:c.7967T=	XP_016869282.1:p.Val2656=
XM_017013794.1:c.7898T=	XP_016869283.1:p.Val2633=
XM_017013795.1:c.7862T=	XP_016869284.1:p.Val2621=
XM_017013796.1:c.7814T=	XP_016869285.1:p.Val2605=
XM_017013797.1:c.7772T=	XP_016869286.1:p.Val2591=
NM_003235.5:c.8033T= MANE Select	NP_003226.4:p.Val2678=