Canonical Allele Identifier: CA1821104936

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133566G= , CM000670.2:g.133133566G=	GRCh38
NC_000008.10:g.134145810G= , CM000670.1:g.134145810G=	GRCh37
NC_000008.9:g.134214992G=	NCBI36
NG_015832.1:g.271606G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8094G= MANE Select	ENSP00000220616.4:p.Lys2698=
ENST00000220616.8:c.8094G=	ENSP00000220616.4:p.Lys2698=
ENST00000519178.5:c.3460G=
ENST00000519543.5:c.2493G=	ENSP00000430430.1:p.Lys831=
ENST00000521107.1:c.306G=	ENSP00000430161.1:p.Lys102=
ENST00000522691.1:n.180G=
ENST00000523756.5:c.4749G=
NM_003235.4:c.8094G=	NP_003226.4:p.Lys2698=
XM_005251038.3:c.7902G=	XP_005251095.1:p.Lys2634=
XM_006716622.2:c.8031G=	XP_006716685.1:p.Lys2677=
XM_005251038.4:c.7902G=	XP_005251095.1:p.Lys2634=
XM_006716622.3:c.8031G=	XP_006716685.1:p.Lys2677=
XM_017013793.1:c.8028G=	XP_016869282.1:p.Lys2676=
XM_017013794.1:c.7959G=	XP_016869283.1:p.Lys2653=
XM_017013795.1:c.7923G=	XP_016869284.1:p.Lys2641=
XM_017013796.1:c.7875G=	XP_016869285.1:p.Lys2625=
XM_017013797.1:c.7833G=	XP_016869286.1:p.Lys2611=
NM_003235.5:c.8094G= MANE Select	NP_003226.4:p.Lys2698=