Canonical Allele Identifier: CA1821104887

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133480T= , CM000670.2:g.133133480T=	GRCh38
NC_000008.10:g.134145724T= , CM000670.1:g.134145724T=	GRCh37
NC_000008.9:g.134214906T=	NCBI36
NG_015832.1:g.271520T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8008T= MANE Select	ENSP00000220616.4:p.Tyr2670=
ENST00000220616.8:c.8008T=	ENSP00000220616.4:p.Tyr2670=
ENST00000519178.5:c.3374T=
ENST00000519543.5:c.2407T=	ENSP00000430430.1:p.Tyr803=
ENST00000521107.1:c.220T=	ENSP00000430161.1:p.Tyr74=
ENST00000522691.1:n.94T=
ENST00000523756.5:c.4663T=
NM_003235.4:c.8008T=	NP_003226.4:p.Tyr2670=
XM_005251038.3:c.7816T=	XP_005251095.1:p.Tyr2606=
XM_006716622.2:c.7945T=	XP_006716685.1:p.Tyr2649=
XM_005251038.4:c.7816T=	XP_005251095.1:p.Tyr2606=
XM_006716622.3:c.7945T=	XP_006716685.1:p.Tyr2649=
XM_017013793.1:c.7942T=	XP_016869282.1:p.Tyr2648=
XM_017013794.1:c.7873T=	XP_016869283.1:p.Tyr2625=
XM_017013795.1:c.7837T=	XP_016869284.1:p.Tyr2613=
XM_017013796.1:c.7789T=	XP_016869285.1:p.Tyr2597=
XM_017013797.1:c.7747T=	XP_016869286.1:p.Tyr2583=
NM_003235.5:c.8008T= MANE Select	NP_003226.4:p.Tyr2670=