Canonical Allele Identifier: CA1821104902

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133513T= , CM000670.2:g.133133513T=	GRCh38
NC_000008.10:g.134145757T= , CM000670.1:g.134145757T=	GRCh37
NC_000008.9:g.134214939T=	NCBI36
NG_015832.1:g.271553T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8041T= MANE Select	ENSP00000220616.4:p.Phe2681=
ENST00000220616.8:c.8041T=	ENSP00000220616.4:p.Phe2681=
ENST00000519178.5:c.3407T=
ENST00000519543.5:c.2440T=	ENSP00000430430.1:p.Phe814=
ENST00000521107.1:c.253T=	ENSP00000430161.1:p.Phe85=
ENST00000522691.1:n.127T=
ENST00000523756.5:c.4696T=
NM_003235.4:c.8041T=	NP_003226.4:p.Phe2681=
XM_005251038.3:c.7849T=	XP_005251095.1:p.Phe2617=
XM_006716622.2:c.7978T=	XP_006716685.1:p.Phe2660=
XM_005251038.4:c.7849T=	XP_005251095.1:p.Phe2617=
XM_006716622.3:c.7978T=	XP_006716685.1:p.Phe2660=
XM_017013793.1:c.7975T=	XP_016869282.1:p.Phe2659=
XM_017013794.1:c.7906T=	XP_016869283.1:p.Phe2636=
XM_017013795.1:c.7870T=	XP_016869284.1:p.Phe2624=
XM_017013796.1:c.7822T=	XP_016869285.1:p.Phe2608=
XM_017013797.1:c.7780T=	XP_016869286.1:p.Phe2594=
NM_003235.5:c.8041T= MANE Select	NP_003226.4:p.Phe2681=