Canonical Allele Identifier: CA463017232

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145852A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133608A>G , CM000670.2:g.133133608A>G	GRCh38
NC_000008.10:g.134145852A>G , CM000670.1:g.134145852A>G	GRCh37
NC_000008.9:g.134215034A>G	NCBI36
NG_015832.1:g.271648A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8136A>G MANE Select	ENSP00000220616.4:p.Lys2712=
ENST00000220616.8:c.8136A>G	ENSP00000220616.4:p.Lys2712=
ENST00000519178.5:c.3502A>G
ENST00000519543.5:c.2535A>G	ENSP00000430430.1:p.Lys845=
ENST00000521107.1:c.348A>G	ENSP00000430161.1:p.Lys116=
ENST00000522691.1:n.222A>G
ENST00000523756.5:c.4791A>G
NM_003235.4:c.8136A>G	NP_003226.4:p.Lys2712=
XM_005251038.3:c.7944A>G	XP_005251095.1:p.Lys2648=
XM_006716622.2:c.8073A>G	XP_006716685.1:p.Lys2691=
XM_005251038.4:c.7944A>G	XP_005251095.1:p.Lys2648=
XM_006716622.3:c.8073A>G	XP_006716685.1:p.Lys2691=
XM_017013793.1:c.8070A>G	XP_016869282.1:p.Lys2690=
XM_017013794.1:c.8001A>G	XP_016869283.1:p.Lys2667=
XM_017013795.1:c.7965A>G	XP_016869284.1:p.Lys2655=
XM_017013796.1:c.7917A>G	XP_016869285.1:p.Lys2639=
XM_017013797.1:c.7875A>G	XP_016869286.1:p.Lys2625=
NM_003235.5:c.8136A>G MANE Select	NP_003226.4:p.Lys2712=