Canonical Allele Identifier: CA1821104926

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133552G= , CM000670.2:g.133133552G=	GRCh38
NC_000008.10:g.134145796G= , CM000670.1:g.134145796G=	GRCh37
NC_000008.9:g.134214978G=	NCBI36
NG_015832.1:g.271592G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8080G= MANE Select	ENSP00000220616.4:p.Gly2694=
ENST00000220616.8:c.8080G=	ENSP00000220616.4:p.Gly2694=
ENST00000519178.5:c.3446G=
ENST00000519543.5:c.2479G=	ENSP00000430430.1:p.Gly827=
ENST00000521107.1:c.292G=	ENSP00000430161.1:p.Gly98=
ENST00000522691.1:n.166G=
ENST00000523756.5:c.4735G=
NM_003235.4:c.8080G=	NP_003226.4:p.Gly2694=
XM_005251038.3:c.7888G=	XP_005251095.1:p.Gly2630=
XM_006716622.2:c.8017G=	XP_006716685.1:p.Gly2673=
XM_005251038.4:c.7888G=	XP_005251095.1:p.Gly2630=
XM_006716622.3:c.8017G=	XP_006716685.1:p.Gly2673=
XM_017013793.1:c.8014G=	XP_016869282.1:p.Gly2672=
XM_017013794.1:c.7945G=	XP_016869283.1:p.Gly2649=
XM_017013795.1:c.7909G=	XP_016869284.1:p.Gly2637=
XM_017013796.1:c.7861G=	XP_016869285.1:p.Gly2621=
XM_017013797.1:c.7819G=	XP_016869286.1:p.Gly2607=
NM_003235.5:c.8080G= MANE Select	NP_003226.4:p.Gly2694=