Canonical Allele Identifier: CA1821104878

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133462T= , CM000670.2:g.133133462T=	GRCh38
NC_000008.10:g.134145706T= , CM000670.1:g.134145706T=	GRCh37
NC_000008.9:g.134214888T=	NCBI36
NG_015832.1:g.271502T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998-8T= MANE Select	ENSP00000220616.4:n.7998-8T=
ENST00000220616.8:c.7998-8T=	ENSP00000220616.4:n.7998-8T=
ENST00000519178.5:c.3364-8T=
ENST00000519543.5:c.2397-8T=	ENSP00000430430.1:n.2397-8T=
ENST00000521107.1:c.210-8T=	ENSP00000430161.1:n.210-8T=
ENST00000522691.1:n.76T=
ENST00000523756.5:c.4653-8T=
NM_003235.4:c.7998-8T=	NP_003226.4:n.7998-8T=
XM_005251038.3:c.7806-8T=	XP_005251095.1:n.7806-8T=
XM_006716622.2:c.7935-8T=	XP_006716685.1:n.7935-8T=
XM_005251038.4:c.7806-8T=	XP_005251095.1:n.7806-8T=
XM_006716622.3:c.7935-8T=	XP_006716685.1:n.7935-8T=
XM_017013793.1:c.7932-8T=	XP_016869282.1:n.7932-8T=
XM_017013794.1:c.7863-8T=	XP_016869283.1:n.7863-8T=
XM_017013795.1:c.7827-8T=	XP_016869284.1:n.7827-8T=
XM_017013796.1:c.7779-8T=	XP_016869285.1:n.7779-8T=
XM_017013797.1:c.7737-8T=	XP_016869286.1:n.7737-8T=
NM_003235.5:c.7998-8T= MANE Select	NP_003226.4:n.7998-8T=