Canonical Allele Identifier: CA463013101

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030237G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017992G>A , CM000670.2:g.133017992G>A	GRCh38
NC_000008.10:g.134030237G>A , CM000670.1:g.134030237G>A	GRCh37
NC_000008.9:g.134099419G>A	NCBI36
NG_015832.1:g.156033G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6777G>A MANE Select	ENSP00000220616.4:p.Lys2259=
ENST00000220616.8:c.6777G>A	ENSP00000220616.4:p.Lys2259=
ENST00000518108.1:c.168+126G>A
ENST00000519178.5:c.2143G>A
ENST00000519543.5:c.1176G>A	ENSP00000430430.1:p.Lys392=
ENST00000523756.5:c.3432G>A
NM_003235.4:c.6777G>A	NP_003226.4:p.Lys2259=
XM_005251038.3:c.6585G>A	XP_005251095.1:p.Lys2195=
XM_006716622.2:c.6714G>A	XP_006716685.1:p.Lys2238=
XM_005251038.4:c.6585G>A	XP_005251095.1:p.Lys2195=
XM_006716622.3:c.6714G>A	XP_006716685.1:p.Lys2238=
XM_017013793.1:c.6711G>A	XP_016869282.1:p.Lys2237=
XM_017013794.1:c.6777G>A	XP_016869283.1:p.Lys2259=
XM_017013795.1:c.6606G>A	XP_016869284.1:p.Lys2202=
XM_017013796.1:c.6558G>A	XP_016869285.1:p.Lys2186=
XM_017013797.1:c.6516G>A	XP_016869286.1:p.Lys2172=
XM_017013798.1:c.6777G>A	XP_016869287.1:p.Lys2259=
NM_003235.5:c.6777G>A MANE Select	NP_003226.4:p.Lys2259=