Canonical Allele Identifier: CA1821104973

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133649A= , CM000670.2:g.133133649A=	GRCh38
NC_000008.10:g.134145893A= , CM000670.1:g.134145893A=	GRCh37
NC_000008.9:g.134215075A=	NCBI36
NG_015832.1:g.271689A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8177A= MANE Select	ENSP00000220616.4:p.Lys2726=
ENST00000220616.8:c.8177A=	ENSP00000220616.4:p.Lys2726=
ENST00000519178.5:c.3543A=
ENST00000519543.5:c.2576A=	ENSP00000430430.1:p.Lys859=
ENST00000521107.1:c.389A=	ENSP00000430161.1:p.Lys130=
ENST00000522691.1:n.263A=
ENST00000523756.5:c.4832A=
NM_003235.4:c.8177A=	NP_003226.4:p.Lys2726=
XM_005251038.3:c.7985A=	XP_005251095.1:p.Lys2662=
XM_006716622.2:c.8114A=	XP_006716685.1:p.Lys2705=
XM_005251038.4:c.7985A=	XP_005251095.1:p.Lys2662=
XM_006716622.3:c.8114A=	XP_006716685.1:p.Lys2705=
XM_017013793.1:c.8111A=	XP_016869282.1:p.Lys2704=
XM_017013794.1:c.8042A=	XP_016869283.1:p.Lys2681=
XM_017013795.1:c.8006A=	XP_016869284.1:p.Lys2669=
XM_017013796.1:c.7958A=	XP_016869285.1:p.Lys2653=
XM_017013797.1:c.7916A=	XP_016869286.1:p.Lys2639=
NM_003235.5:c.8177A= MANE Select	NP_003226.4:p.Lys2726=