Canonical Allele Identifier: CA1821104937

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133568A= , CM000670.2:g.133133568A=	GRCh38
NC_000008.10:g.134145812A= , CM000670.1:g.134145812A=	GRCh37
NC_000008.9:g.134214994A=	NCBI36
NG_015832.1:g.271608A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8096A= MANE Select	ENSP00000220616.4:p.Glu2699=
ENST00000220616.8:c.8096A=	ENSP00000220616.4:p.Glu2699=
ENST00000519178.5:c.3462A=
ENST00000519543.5:c.2495A=	ENSP00000430430.1:p.Glu832=
ENST00000521107.1:c.308A=	ENSP00000430161.1:p.Glu103=
ENST00000522691.1:n.182A=
ENST00000523756.5:c.4751A=
NM_003235.4:c.8096A=	NP_003226.4:p.Glu2699=
XM_005251038.3:c.7904A=	XP_005251095.1:p.Glu2635=
XM_006716622.2:c.8033A=	XP_006716685.1:p.Glu2678=
XM_005251038.4:c.7904A=	XP_005251095.1:p.Glu2635=
XM_006716622.3:c.8033A=	XP_006716685.1:p.Glu2678=
XM_017013793.1:c.8030A=	XP_016869282.1:p.Glu2677=
XM_017013794.1:c.7961A=	XP_016869283.1:p.Glu2654=
XM_017013795.1:c.7925A=	XP_016869284.1:p.Glu2642=
XM_017013796.1:c.7877A=	XP_016869285.1:p.Glu2626=
XM_017013797.1:c.7835A=	XP_016869286.1:p.Glu2612=
NM_003235.5:c.8096A= MANE Select	NP_003226.4:p.Glu2699=