Canonical Allele Identifier: CA1821104945

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133589A= , CM000670.2:g.133133589A=	GRCh38
NC_000008.10:g.134145833A= , CM000670.1:g.134145833A=	GRCh37
NC_000008.9:g.134215015A=	NCBI36
NG_015832.1:g.271629A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8117A= MANE Select	ENSP00000220616.4:p.Asn2706=
ENST00000220616.8:c.8117A=	ENSP00000220616.4:p.Asn2706=
ENST00000519178.5:c.3483A=
ENST00000519543.5:c.2516A=	ENSP00000430430.1:p.Asn839=
ENST00000521107.1:c.329A=	ENSP00000430161.1:p.Asn110=
ENST00000522691.1:n.203A=
ENST00000523756.5:c.4772A=
NM_003235.4:c.8117A=	NP_003226.4:p.Asn2706=
XM_005251038.3:c.7925A=	XP_005251095.1:p.Asn2642=
XM_006716622.2:c.8054A=	XP_006716685.1:p.Asn2685=
XM_005251038.4:c.7925A=	XP_005251095.1:p.Asn2642=
XM_006716622.3:c.8054A=	XP_006716685.1:p.Asn2685=
XM_017013793.1:c.8051A=	XP_016869282.1:p.Asn2684=
XM_017013794.1:c.7982A=	XP_016869283.1:p.Asn2661=
XM_017013795.1:c.7946A=	XP_016869284.1:p.Asn2649=
XM_017013796.1:c.7898A=	XP_016869285.1:p.Asn2633=
XM_017013797.1:c.7856A=	XP_016869286.1:p.Asn2619=
NM_003235.5:c.8117A= MANE Select	NP_003226.4:p.Asn2706=