Canonical Allele Identifier: CA1821104913

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133532A= , CM000670.2:g.133133532A=	GRCh38
NC_000008.10:g.134145776A= , CM000670.1:g.134145776A=	GRCh37
NC_000008.9:g.134214958A=	NCBI36
NG_015832.1:g.271572A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8060A= MANE Select	ENSP00000220616.4:p.Asp2687=
ENST00000220616.8:c.8060A=	ENSP00000220616.4:p.Asp2687=
ENST00000519178.5:c.3426A=
ENST00000519543.5:c.2459A=	ENSP00000430430.1:p.Asp820=
ENST00000521107.1:c.272A=	ENSP00000430161.1:p.Asp91=
ENST00000522691.1:n.146A=
ENST00000523756.5:c.4715A=
NM_003235.4:c.8060A=	NP_003226.4:p.Asp2687=
XM_005251038.3:c.7868A=	XP_005251095.1:p.Asp2623=
XM_006716622.2:c.7997A=	XP_006716685.1:p.Asp2666=
XM_005251038.4:c.7868A=	XP_005251095.1:p.Asp2623=
XM_006716622.3:c.7997A=	XP_006716685.1:p.Asp2666=
XM_017013793.1:c.7994A=	XP_016869282.1:p.Asp2665=
XM_017013794.1:c.7925A=	XP_016869283.1:p.Asp2642=
XM_017013795.1:c.7889A=	XP_016869284.1:p.Asp2630=
XM_017013796.1:c.7841A=	XP_016869285.1:p.Asp2614=
XM_017013797.1:c.7799A=	XP_016869286.1:p.Asp2600=
NM_003235.5:c.8060A= MANE Select	NP_003226.4:p.Asp2687=