Canonical Allele Identifier: CA1821104919

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133541C= , CM000670.2:g.133133541C=	GRCh38
NC_000008.10:g.134145785C= , CM000670.1:g.134145785C=	GRCh37
NC_000008.9:g.134214967C=	NCBI36
NG_015832.1:g.271581C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8069C= MANE Select	ENSP00000220616.4:p.Pro2690=
ENST00000220616.8:c.8069C=	ENSP00000220616.4:p.Pro2690=
ENST00000519178.5:c.3435C=
ENST00000519543.5:c.2468C=	ENSP00000430430.1:p.Pro823=
ENST00000521107.1:c.281C=	ENSP00000430161.1:p.Pro94=
ENST00000522691.1:n.155C=
ENST00000523756.5:c.4724C=
NM_003235.4:c.8069C=	NP_003226.4:p.Pro2690=
XM_005251038.3:c.7877C=	XP_005251095.1:p.Pro2626=
XM_006716622.2:c.8006C=	XP_006716685.1:p.Pro2669=
XM_005251038.4:c.7877C=	XP_005251095.1:p.Pro2626=
XM_006716622.3:c.8006C=	XP_006716685.1:p.Pro2669=
XM_017013793.1:c.8003C=	XP_016869282.1:p.Pro2668=
XM_017013794.1:c.7934C=	XP_016869283.1:p.Pro2645=
XM_017013795.1:c.7898C=	XP_016869284.1:p.Pro2633=
XM_017013796.1:c.7850C=	XP_016869285.1:p.Pro2617=
XM_017013797.1:c.7808C=	XP_016869286.1:p.Pro2603=
NM_003235.5:c.8069C= MANE Select	NP_003226.4:p.Pro2690=