Canonical Allele Identifier: CA1821104946

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133590T= , CM000670.2:g.133133590T=	GRCh38
NC_000008.10:g.134145834T= , CM000670.1:g.134145834T=	GRCh37
NC_000008.9:g.134215016T=	NCBI36
NG_015832.1:g.271630T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8118T= MANE Select	ENSP00000220616.4:p.Asn2706=
ENST00000220616.8:c.8118T=	ENSP00000220616.4:p.Asn2706=
ENST00000519178.5:c.3484T=
ENST00000519543.5:c.2517T=	ENSP00000430430.1:p.Asn839=
ENST00000521107.1:c.330T=	ENSP00000430161.1:p.Asn110=
ENST00000522691.1:n.204T=
ENST00000523756.5:c.4773T=
NM_003235.4:c.8118T=	NP_003226.4:p.Asn2706=
XM_005251038.3:c.7926T=	XP_005251095.1:p.Asn2642=
XM_006716622.2:c.8055T=	XP_006716685.1:p.Asn2685=
XM_005251038.4:c.7926T=	XP_005251095.1:p.Asn2642=
XM_006716622.3:c.8055T=	XP_006716685.1:p.Asn2685=
XM_017013793.1:c.8052T=	XP_016869282.1:p.Asn2684=
XM_017013794.1:c.7983T=	XP_016869283.1:p.Asn2661=
XM_017013795.1:c.7947T=	XP_016869284.1:p.Asn2649=
XM_017013796.1:c.7899T=	XP_016869285.1:p.Asn2633=
XM_017013797.1:c.7857T=	XP_016869286.1:p.Asn2619=
NM_003235.5:c.8118T= MANE Select	NP_003226.4:p.Asn2706=