Canonical Allele Identifier: CA1821104956

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133612G= , CM000670.2:g.133133612G=	GRCh38
NC_000008.10:g.134145856G= , CM000670.1:g.134145856G=	GRCh37
NC_000008.9:g.134215038G=	NCBI36
NG_015832.1:g.271652G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8140G= MANE Select	ENSP00000220616.4:p.Asp2714=
ENST00000220616.8:c.8140G=	ENSP00000220616.4:p.Asp2714=
ENST00000519178.5:c.3506G=
ENST00000519543.5:c.2539G=	ENSP00000430430.1:p.Asp847=
ENST00000521107.1:c.352G=	ENSP00000430161.1:p.Asp118=
ENST00000522691.1:n.226G=
ENST00000523756.5:c.4795G=
NM_003235.4:c.8140G=	NP_003226.4:p.Asp2714=
XM_005251038.3:c.7948G=	XP_005251095.1:p.Asp2650=
XM_006716622.2:c.8077G=	XP_006716685.1:p.Asp2693=
XM_005251038.4:c.7948G=	XP_005251095.1:p.Asp2650=
XM_006716622.3:c.8077G=	XP_006716685.1:p.Asp2693=
XM_017013793.1:c.8074G=	XP_016869282.1:p.Asp2692=
XM_017013794.1:c.8005G=	XP_016869283.1:p.Asp2669=
XM_017013795.1:c.7969G=	XP_016869284.1:p.Asp2657=
XM_017013796.1:c.7921G=	XP_016869285.1:p.Asp2641=
XM_017013797.1:c.7879G=	XP_016869286.1:p.Asp2627=
NM_003235.5:c.8140G= MANE Select	NP_003226.4:p.Asp2714=