Canonical Allele Identifier: CA1821104888

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133481A= , CM000670.2:g.133133481A=	GRCh38
NC_000008.10:g.134145725A= , CM000670.1:g.134145725A=	GRCh37
NC_000008.9:g.134214907A=	NCBI36
NG_015832.1:g.271521A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8009A= MANE Select	ENSP00000220616.4:p.Tyr2670=
ENST00000220616.8:c.8009A=	ENSP00000220616.4:p.Tyr2670=
ENST00000519178.5:c.3375A=
ENST00000519543.5:c.2408A=	ENSP00000430430.1:p.Tyr803=
ENST00000521107.1:c.221A=	ENSP00000430161.1:p.Tyr74=
ENST00000522691.1:n.95A=
ENST00000523756.5:c.4664A=
NM_003235.4:c.8009A=	NP_003226.4:p.Tyr2670=
XM_005251038.3:c.7817A=	XP_005251095.1:p.Tyr2606=
XM_006716622.2:c.7946A=	XP_006716685.1:p.Tyr2649=
XM_005251038.4:c.7817A=	XP_005251095.1:p.Tyr2606=
XM_006716622.3:c.7946A=	XP_006716685.1:p.Tyr2649=
XM_017013793.1:c.7943A=	XP_016869282.1:p.Tyr2648=
XM_017013794.1:c.7874A=	XP_016869283.1:p.Tyr2625=
XM_017013795.1:c.7838A=	XP_016869284.1:p.Tyr2613=
XM_017013796.1:c.7790A=	XP_016869285.1:p.Tyr2597=
XM_017013797.1:c.7748A=	XP_016869286.1:p.Tyr2583=
NM_003235.5:c.8009A= MANE Select	NP_003226.4:p.Tyr2670=