Canonical Allele Identifier: CA1821104943

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133583T= , CM000670.2:g.133133583T=	GRCh38
NC_000008.10:g.134145827T= , CM000670.1:g.134145827T=	GRCh37
NC_000008.9:g.134215009T=	NCBI36
NG_015832.1:g.271623T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8111T= MANE Select	ENSP00000220616.4:p.Leu2704=
ENST00000220616.8:c.8111T=	ENSP00000220616.4:p.Leu2704=
ENST00000519178.5:c.3477T=
ENST00000519543.5:c.2510T=	ENSP00000430430.1:p.Leu837=
ENST00000521107.1:c.323T=	ENSP00000430161.1:p.Leu108=
ENST00000522691.1:n.197T=
ENST00000523756.5:c.4766T=
NM_003235.4:c.8111T=	NP_003226.4:p.Leu2704=
XM_005251038.3:c.7919T=	XP_005251095.1:p.Leu2640=
XM_006716622.2:c.8048T=	XP_006716685.1:p.Leu2683=
XM_005251038.4:c.7919T=	XP_005251095.1:p.Leu2640=
XM_006716622.3:c.8048T=	XP_006716685.1:p.Leu2683=
XM_017013793.1:c.8045T=	XP_016869282.1:p.Leu2682=
XM_017013794.1:c.7976T=	XP_016869283.1:p.Leu2659=
XM_017013795.1:c.7940T=	XP_016869284.1:p.Leu2647=
XM_017013796.1:c.7892T=	XP_016869285.1:p.Leu2631=
XM_017013797.1:c.7850T=	XP_016869286.1:p.Leu2617=
NM_003235.5:c.8111T= MANE Select	NP_003226.4:p.Leu2704=