Canonical Allele Identifier: CA1821104928

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133556A= , CM000670.2:g.133133556A=	GRCh38
NC_000008.10:g.134145800A= , CM000670.1:g.134145800A=	GRCh37
NC_000008.9:g.134214982A=	NCBI36
NG_015832.1:g.271596A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8084A= MANE Select	ENSP00000220616.4:p.Glu2695=
ENST00000220616.8:c.8084A=	ENSP00000220616.4:p.Glu2695=
ENST00000519178.5:c.3450A=
ENST00000519543.5:c.2483A=	ENSP00000430430.1:p.Glu828=
ENST00000521107.1:c.296A=	ENSP00000430161.1:p.Glu99=
ENST00000522691.1:n.170A=
ENST00000523756.5:c.4739A=
NM_003235.4:c.8084A=	NP_003226.4:p.Glu2695=
XM_005251038.3:c.7892A=	XP_005251095.1:p.Glu2631=
XM_006716622.2:c.8021A=	XP_006716685.1:p.Glu2674=
XM_005251038.4:c.7892A=	XP_005251095.1:p.Glu2631=
XM_006716622.3:c.8021A=	XP_006716685.1:p.Glu2674=
XM_017013793.1:c.8018A=	XP_016869282.1:p.Glu2673=
XM_017013794.1:c.7949A=	XP_016869283.1:p.Glu2650=
XM_017013795.1:c.7913A=	XP_016869284.1:p.Glu2638=
XM_017013796.1:c.7865A=	XP_016869285.1:p.Glu2622=
XM_017013797.1:c.7823A=	XP_016869286.1:p.Glu2608=
NM_003235.5:c.8084A= MANE Select	NP_003226.4:p.Glu2695=