Canonical Allele Identifier: CA1821104960

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133622T= , CM000670.2:g.133133622T=	GRCh38
NC_000008.10:g.134145866T= , CM000670.1:g.134145866T=	GRCh37
NC_000008.9:g.134215048T=	NCBI36
NG_015832.1:g.271662T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8150T= MANE Select	ENSP00000220616.4:p.Phe2717=
ENST00000220616.8:c.8150T=	ENSP00000220616.4:p.Phe2717=
ENST00000519178.5:c.3516T=
ENST00000519543.5:c.2549T=	ENSP00000430430.1:p.Phe850=
ENST00000521107.1:c.362T=	ENSP00000430161.1:p.Phe121=
ENST00000522691.1:n.236T=
ENST00000523756.5:c.4805T=
NM_003235.4:c.8150T=	NP_003226.4:p.Phe2717=
XM_005251038.3:c.7958T=	XP_005251095.1:p.Phe2653=
XM_006716622.2:c.8087T=	XP_006716685.1:p.Phe2696=
XM_005251038.4:c.7958T=	XP_005251095.1:p.Phe2653=
XM_006716622.3:c.8087T=	XP_006716685.1:p.Phe2696=
XM_017013793.1:c.8084T=	XP_016869282.1:p.Phe2695=
XM_017013794.1:c.8015T=	XP_016869283.1:p.Phe2672=
XM_017013795.1:c.7979T=	XP_016869284.1:p.Phe2660=
XM_017013796.1:c.7931T=	XP_016869285.1:p.Phe2644=
XM_017013797.1:c.7889T=	XP_016869286.1:p.Phe2630=
NM_003235.5:c.8150T= MANE Select	NP_003226.4:p.Phe2717=