Canonical Allele Identifier: CA1821046474

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017994C= , CM000670.2:g.133017994C=	GRCh38
NC_000008.10:g.134030239C= , CM000670.1:g.134030239C=	GRCh37
NC_000008.9:g.134099421C=	NCBI36
NG_015832.1:g.156035C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6779C= MANE Select	ENSP00000220616.4:p.Pro2260=
ENST00000220616.8:c.6779C=	ENSP00000220616.4:p.Pro2260=
ENST00000518108.1:c.168+128C=
ENST00000519178.5:c.2145C=
ENST00000519543.5:c.1178C=	ENSP00000430430.1:p.Pro393=
ENST00000523756.5:c.3434C=
NM_003235.4:c.6779C=	NP_003226.4:p.Pro2260=
XM_005251038.3:c.6587C=	XP_005251095.1:p.Pro2196=
XM_006716622.2:c.6716C=	XP_006716685.1:p.Pro2239=
XM_005251038.4:c.6587C=	XP_005251095.1:p.Pro2196=
XM_006716622.3:c.6716C=	XP_006716685.1:p.Pro2239=
XM_017013793.1:c.6713C=	XP_016869282.1:p.Pro2238=
XM_017013794.1:c.6779C=	XP_016869283.1:p.Pro2260=
XM_017013795.1:c.6608C=	XP_016869284.1:p.Pro2203=
XM_017013796.1:c.6560C=	XP_016869285.1:p.Pro2187=
XM_017013797.1:c.6518C=	XP_016869286.1:p.Pro2173=
XM_017013798.1:c.6779C=	XP_016869287.1:p.Pro2260=
NM_003235.5:c.6779C= MANE Select	NP_003226.4:p.Pro2260=