Canonical Allele Identifier: CA1821104910

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133527G= , CM000670.2:g.133133527G=	GRCh38
NC_000008.10:g.134145771G= , CM000670.1:g.134145771G=	GRCh37
NC_000008.9:g.134214953G=	NCBI36
NG_015832.1:g.271567G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8055G= MANE Select	ENSP00000220616.4:p.Trp2685=
ENST00000220616.8:c.8055G=	ENSP00000220616.4:p.Trp2685=
ENST00000519178.5:c.3421G=
ENST00000519543.5:c.2454G=	ENSP00000430430.1:p.Trp818=
ENST00000521107.1:c.267G=	ENSP00000430161.1:p.Trp89=
ENST00000522691.1:n.141G=
ENST00000523756.5:c.4710G=
NM_003235.4:c.8055G=	NP_003226.4:p.Trp2685=
XM_005251038.3:c.7863G=	XP_005251095.1:p.Trp2621=
XM_006716622.2:c.7992G=	XP_006716685.1:p.Trp2664=
XM_005251038.4:c.7863G=	XP_005251095.1:p.Trp2621=
XM_006716622.3:c.7992G=	XP_006716685.1:p.Trp2664=
XM_017013793.1:c.7989G=	XP_016869282.1:p.Trp2663=
XM_017013794.1:c.7920G=	XP_016869283.1:p.Trp2640=
XM_017013795.1:c.7884G=	XP_016869284.1:p.Trp2628=
XM_017013796.1:c.7836G=	XP_016869285.1:p.Trp2612=
XM_017013797.1:c.7794G=	XP_016869286.1:p.Trp2598=
NM_003235.5:c.8055G= MANE Select	NP_003226.4:p.Trp2685=