Canonical Allele Identifier: CA1821104948

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133592G= , CM000670.2:g.133133592G=	GRCh38
NC_000008.10:g.134145836G= , CM000670.1:g.134145836G=	GRCh37
NC_000008.9:g.134215018G=	NCBI36
NG_015832.1:g.271632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8120G= MANE Select	ENSP00000220616.4:p.Arg2707=
ENST00000220616.8:c.8120G=	ENSP00000220616.4:p.Arg2707=
ENST00000519178.5:c.3486G=
ENST00000519543.5:c.2519G=	ENSP00000430430.1:p.Arg840=
ENST00000521107.1:c.332G=	ENSP00000430161.1:p.Arg111=
ENST00000522691.1:n.206G=
ENST00000523756.5:c.4775G=
NM_003235.4:c.8120G=	NP_003226.4:p.Arg2707=
XM_005251038.3:c.7928G=	XP_005251095.1:p.Arg2643=
XM_006716622.2:c.8057G=	XP_006716685.1:p.Arg2686=
XM_005251038.4:c.7928G=	XP_005251095.1:p.Arg2643=
XM_006716622.3:c.8057G=	XP_006716685.1:p.Arg2686=
XM_017013793.1:c.8054G=	XP_016869282.1:p.Arg2685=
XM_017013794.1:c.7985G=	XP_016869283.1:p.Arg2662=
XM_017013795.1:c.7949G=	XP_016869284.1:p.Arg2650=
XM_017013796.1:c.7901G=	XP_016869285.1:p.Arg2634=
XM_017013797.1:c.7859G=	XP_016869286.1:p.Arg2620=
NM_003235.5:c.8120G= MANE Select	NP_003226.4:p.Arg2707=