Canonical Allele Identifier: CA1821104957

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133616G= , CM000670.2:g.133133616G=	GRCh38
NC_000008.10:g.134145860G= , CM000670.1:g.134145860G=	GRCh37
NC_000008.9:g.134215042G=	NCBI36
NG_015832.1:g.271656G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8144G= MANE Select	ENSP00000220616.4:p.Cys2715=
ENST00000220616.8:c.8144G=	ENSP00000220616.4:p.Cys2715=
ENST00000519178.5:c.3510G=
ENST00000519543.5:c.2543G=	ENSP00000430430.1:p.Cys848=
ENST00000521107.1:c.356G=	ENSP00000430161.1:p.Cys119=
ENST00000522691.1:n.230G=
ENST00000523756.5:c.4799G=
NM_003235.4:c.8144G=	NP_003226.4:p.Cys2715=
XM_005251038.3:c.7952G=	XP_005251095.1:p.Cys2651=
XM_006716622.2:c.8081G=	XP_006716685.1:p.Cys2694=
XM_005251038.4:c.7952G=	XP_005251095.1:p.Cys2651=
XM_006716622.3:c.8081G=	XP_006716685.1:p.Cys2694=
XM_017013793.1:c.8078G=	XP_016869282.1:p.Cys2693=
XM_017013794.1:c.8009G=	XP_016869283.1:p.Cys2670=
XM_017013795.1:c.7973G=	XP_016869284.1:p.Cys2658=
XM_017013796.1:c.7925G=	XP_016869285.1:p.Cys2642=
XM_017013797.1:c.7883G=	XP_016869286.1:p.Cys2628=
NM_003235.5:c.8144G= MANE Select	NP_003226.4:p.Cys2715=