Canonical Allele Identifier: CA1821104927

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133555G= , CM000670.2:g.133133555G=	GRCh38
NC_000008.10:g.134145799G= , CM000670.1:g.134145799G=	GRCh37
NC_000008.9:g.134214981G=	NCBI36
NG_015832.1:g.271595G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8083G= MANE Select	ENSP00000220616.4:p.Glu2695=
ENST00000220616.8:c.8083G=	ENSP00000220616.4:p.Glu2695=
ENST00000519178.5:c.3449G=
ENST00000519543.5:c.2482G=	ENSP00000430430.1:p.Glu828=
ENST00000521107.1:c.295G=	ENSP00000430161.1:p.Glu99=
ENST00000522691.1:n.169G=
ENST00000523756.5:c.4738G=
NM_003235.4:c.8083G=	NP_003226.4:p.Glu2695=
XM_005251038.3:c.7891G=	XP_005251095.1:p.Glu2631=
XM_006716622.2:c.8020G=	XP_006716685.1:p.Glu2674=
XM_005251038.4:c.7891G=	XP_005251095.1:p.Glu2631=
XM_006716622.3:c.8020G=	XP_006716685.1:p.Glu2674=
XM_017013793.1:c.8017G=	XP_016869282.1:p.Glu2673=
XM_017013794.1:c.7948G=	XP_016869283.1:p.Glu2650=
XM_017013795.1:c.7912G=	XP_016869284.1:p.Glu2638=
XM_017013796.1:c.7864G=	XP_016869285.1:p.Glu2622=
XM_017013797.1:c.7822G=	XP_016869286.1:p.Glu2608=
NM_003235.5:c.8083G= MANE Select	NP_003226.4:p.Glu2695=