Canonical Allele Identifier: CA1821104889

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133482C= , CM000670.2:g.133133482C=	GRCh38
NC_000008.10:g.134145726C= , CM000670.1:g.134145726C=	GRCh37
NC_000008.9:g.134214908C=	NCBI36
NG_015832.1:g.271522C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8010C= MANE Select	ENSP00000220616.4:p.Tyr2670=
ENST00000220616.8:c.8010C=	ENSP00000220616.4:p.Tyr2670=
ENST00000519178.5:c.3376C=
ENST00000519543.5:c.2409C=	ENSP00000430430.1:p.Tyr803=
ENST00000521107.1:c.222C=	ENSP00000430161.1:p.Tyr74=
ENST00000522691.1:n.96C=
ENST00000523756.5:c.4665C=
NM_003235.4:c.8010C=	NP_003226.4:p.Tyr2670=
XM_005251038.3:c.7818C=	XP_005251095.1:p.Tyr2606=
XM_006716622.2:c.7947C=	XP_006716685.1:p.Tyr2649=
XM_005251038.4:c.7818C=	XP_005251095.1:p.Tyr2606=
XM_006716622.3:c.7947C=	XP_006716685.1:p.Tyr2649=
XM_017013793.1:c.7944C=	XP_016869282.1:p.Tyr2648=
XM_017013794.1:c.7875C=	XP_016869283.1:p.Tyr2625=
XM_017013795.1:c.7839C=	XP_016869284.1:p.Tyr2613=
XM_017013796.1:c.7791C=	XP_016869285.1:p.Tyr2597=
XM_017013797.1:c.7749C=	XP_016869286.1:p.Tyr2583=
NM_003235.5:c.8010C= MANE Select	NP_003226.4:p.Tyr2670=