Canonical Allele Identifier: CA1821104954

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133609G= , CM000670.2:g.133133609G=	GRCh38
NC_000008.10:g.134145853G= , CM000670.1:g.134145853G=	GRCh37
NC_000008.9:g.134215035G=	NCBI36
NG_015832.1:g.271649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8137G= MANE Select	ENSP00000220616.4:p.Ala2713=
ENST00000220616.8:c.8137G=	ENSP00000220616.4:p.Ala2713=
ENST00000519178.5:c.3503G=
ENST00000519543.5:c.2536G=	ENSP00000430430.1:p.Ala846=
ENST00000521107.1:c.349G=	ENSP00000430161.1:p.Ala117=
ENST00000522691.1:n.223G=
ENST00000523756.5:c.4792G=
NM_003235.4:c.8137G=	NP_003226.4:p.Ala2713=
XM_005251038.3:c.7945G=	XP_005251095.1:p.Ala2649=
XM_006716622.2:c.8074G=	XP_006716685.1:p.Ala2692=
XM_005251038.4:c.7945G=	XP_005251095.1:p.Ala2649=
XM_006716622.3:c.8074G=	XP_006716685.1:p.Ala2692=
XM_017013793.1:c.8071G=	XP_016869282.1:p.Ala2691=
XM_017013794.1:c.8002G=	XP_016869283.1:p.Ala2668=
XM_017013795.1:c.7966G=	XP_016869284.1:p.Ala2656=
XM_017013796.1:c.7918G=	XP_016869285.1:p.Ala2640=
XM_017013797.1:c.7876G=	XP_016869286.1:p.Ala2626=
NM_003235.5:c.8137G= MANE Select	NP_003226.4:p.Ala2713=