Canonical Allele Identifier: CA1821104912

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133530T= , CM000670.2:g.133133530T=	GRCh38
NC_000008.10:g.134145774T= , CM000670.1:g.134145774T=	GRCh37
NC_000008.9:g.134214956T=	NCBI36
NG_015832.1:g.271570T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8058T= MANE Select	ENSP00000220616.4:p.Pro2686=
ENST00000220616.8:c.8058T=	ENSP00000220616.4:p.Pro2686=
ENST00000519178.5:c.3424T=
ENST00000519543.5:c.2457T=	ENSP00000430430.1:p.Pro819=
ENST00000521107.1:c.270T=	ENSP00000430161.1:p.Pro90=
ENST00000522691.1:n.144T=
ENST00000523756.5:c.4713T=
NM_003235.4:c.8058T=	NP_003226.4:p.Pro2686=
XM_005251038.3:c.7866T=	XP_005251095.1:p.Pro2622=
XM_006716622.2:c.7995T=	XP_006716685.1:p.Pro2665=
XM_005251038.4:c.7866T=	XP_005251095.1:p.Pro2622=
XM_006716622.3:c.7995T=	XP_006716685.1:p.Pro2665=
XM_017013793.1:c.7992T=	XP_016869282.1:p.Pro2664=
XM_017013794.1:c.7923T=	XP_016869283.1:p.Pro2641=
XM_017013795.1:c.7887T=	XP_016869284.1:p.Pro2629=
XM_017013796.1:c.7839T=	XP_016869285.1:p.Pro2613=
XM_017013797.1:c.7797T=	XP_016869286.1:p.Pro2599=
NM_003235.5:c.8058T= MANE Select	NP_003226.4:p.Pro2686=