Canonical Allele Identifier: CA1821104916

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133537G= , CM000670.2:g.133133537G=	GRCh38
NC_000008.10:g.134145781G= , CM000670.1:g.134145781G=	GRCh37
NC_000008.9:g.134214963G=	NCBI36
NG_015832.1:g.271577G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8065G= MANE Select	ENSP00000220616.4:p.Val2689=
ENST00000220616.8:c.8065G=	ENSP00000220616.4:p.Val2689=
ENST00000519178.5:c.3431G=
ENST00000519543.5:c.2464G=	ENSP00000430430.1:p.Val822=
ENST00000521107.1:c.277G=	ENSP00000430161.1:p.Val93=
ENST00000522691.1:n.151G=
ENST00000523756.5:c.4720G=
NM_003235.4:c.8065G=	NP_003226.4:p.Val2689=
XM_005251038.3:c.7873G=	XP_005251095.1:p.Val2625=
XM_006716622.2:c.8002G=	XP_006716685.1:p.Val2668=
XM_005251038.4:c.7873G=	XP_005251095.1:p.Val2625=
XM_006716622.3:c.8002G=	XP_006716685.1:p.Val2668=
XM_017013793.1:c.7999G=	XP_016869282.1:p.Val2667=
XM_017013794.1:c.7930G=	XP_016869283.1:p.Val2644=
XM_017013795.1:c.7894G=	XP_016869284.1:p.Val2632=
XM_017013796.1:c.7846G=	XP_016869285.1:p.Val2616=
XM_017013797.1:c.7804G=	XP_016869286.1:p.Val2602=
NM_003235.5:c.8065G= MANE Select	NP_003226.4:p.Val2689=