Canonical Allele Identifier: CA1821104931

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133559A= , CM000670.2:g.133133559A=	GRCh38
NC_000008.10:g.134145803A= , CM000670.1:g.134145803A=	GRCh37
NC_000008.9:g.134214985A=	NCBI36
NG_015832.1:g.271599A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8087A= MANE Select	ENSP00000220616.4:p.Asn2696=
ENST00000220616.8:c.8087A=	ENSP00000220616.4:p.Asn2696=
ENST00000519178.5:c.3453A=
ENST00000519543.5:c.2486A=	ENSP00000430430.1:p.Asn829=
ENST00000521107.1:c.299A=	ENSP00000430161.1:p.Asn100=
ENST00000522691.1:n.173A=
ENST00000523756.5:c.4742A=
NM_003235.4:c.8087A=	NP_003226.4:p.Asn2696=
XM_005251038.3:c.7895A=	XP_005251095.1:p.Asn2632=
XM_006716622.2:c.8024A=	XP_006716685.1:p.Asn2675=
XM_005251038.4:c.7895A=	XP_005251095.1:p.Asn2632=
XM_006716622.3:c.8024A=	XP_006716685.1:p.Asn2675=
XM_017013793.1:c.8021A=	XP_016869282.1:p.Asn2674=
XM_017013794.1:c.7952A=	XP_016869283.1:p.Asn2651=
XM_017013795.1:c.7916A=	XP_016869284.1:p.Asn2639=
XM_017013796.1:c.7868A=	XP_016869285.1:p.Asn2623=
XM_017013797.1:c.7826A=	XP_016869286.1:p.Asn2609=
NM_003235.5:c.8087A= MANE Select	NP_003226.4:p.Asn2696=