Canonical Allele Identifier: CA1821104838

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133384T= , CM000670.2:g.133133384T=	GRCh38
NC_000008.10:g.134145628T= , CM000670.1:g.134145628T=	GRCh37
NC_000008.9:g.134214810T=	NCBI36
NG_015832.1:g.271424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998-86T= MANE Select	ENSP00000220616.4:n.7998-86T=
ENST00000220616.8:c.7998-86T=	ENSP00000220616.4:n.7998-86T=
ENST00000519178.5:c.3364-86T=
ENST00000519543.5:c.2397-86T=	ENSP00000430430.1:n.2397-86T=
ENST00000521107.1:c.210-86T=	ENSP00000430161.1:n.210-86T=
ENST00000523756.5:c.4653-86T=
NM_003235.4:c.7998-86T=	NP_003226.4:n.7998-86T=
XM_005251038.3:c.7806-86T=	XP_005251095.1:n.7806-86T=
XM_006716622.2:c.7935-86T=	XP_006716685.1:n.7935-86T=
XM_005251038.4:c.7806-86T=	XP_005251095.1:n.7806-86T=
XM_006716622.3:c.7935-86T=	XP_006716685.1:n.7935-86T=
XM_017013793.1:c.7932-86T=	XP_016869282.1:n.7932-86T=
XM_017013794.1:c.7863-86T=	XP_016869283.1:n.7863-86T=
XM_017013795.1:c.7827-86T=	XP_016869284.1:n.7827-86T=
XM_017013796.1:c.7779-86T=	XP_016869285.1:n.7779-86T=
XM_017013797.1:c.7737-86T=	XP_016869286.1:n.7737-86T=
NM_003235.5:c.7998-86T= MANE Select	NP_003226.4:n.7998-86T=