Canonical Allele Identifier: CA1821104966

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133635C= , CM000670.2:g.133133635C=	GRCh38
NC_000008.10:g.134145879C= , CM000670.1:g.134145879C=	GRCh37
NC_000008.9:g.134215061C=	NCBI36
NG_015832.1:g.271675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8163C= MANE Select	ENSP00000220616.4:p.Tyr2721=
ENST00000220616.8:c.8163C=	ENSP00000220616.4:p.Tyr2721=
ENST00000519178.5:c.3529C=
ENST00000519543.5:c.2562C=	ENSP00000430430.1:p.Tyr854=
ENST00000521107.1:c.375C=	ENSP00000430161.1:p.Tyr125=
ENST00000522691.1:n.249C=
ENST00000523756.5:c.4818C=
NM_003235.4:c.8163C=	NP_003226.4:p.Tyr2721=
XM_005251038.3:c.7971C=	XP_005251095.1:p.Tyr2657=
XM_006716622.2:c.8100C=	XP_006716685.1:p.Tyr2700=
XM_005251038.4:c.7971C=	XP_005251095.1:p.Tyr2657=
XM_006716622.3:c.8100C=	XP_006716685.1:p.Tyr2700=
XM_017013793.1:c.8097C=	XP_016869282.1:p.Tyr2699=
XM_017013794.1:c.8028C=	XP_016869283.1:p.Tyr2676=
XM_017013795.1:c.7992C=	XP_016869284.1:p.Tyr2664=
XM_017013796.1:c.7944C=	XP_016869285.1:p.Tyr2648=
XM_017013797.1:c.7902C=	XP_016869286.1:p.Tyr2634=
NM_003235.5:c.8163C= MANE Select	NP_003226.4:p.Tyr2721=