Canonical Allele Identifier: CA372234002

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133980051A>G (hg19) ; chr8:g.132967806A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132967806A>G , CM000670.2:g.132967806A>G	GRCh38
NC_000008.10:g.133980051A>G , CM000670.1:g.133980051A>G	GRCh37
NC_000008.9:g.134049233A>G	NCBI36
NG_015832.1:g.105847A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5699A>G MANE Select	ENSP00000220616.4:p.Glu1900Gly
ENST00000220616.8:c.5699A>G	ENSP00000220616.4:p.Glu1900Gly
ENST00000518058.1:c.94A>G
ENST00000519178.5:c.1065A>G
ENST00000519543.5:c.161A>G	ENSP00000430430.1:p.Glu54Gly
ENST00000523756.5:c.2354A>G
NM_003235.4:c.5699A>G	NP_003226.4:p.Glu1900Gly
XM_005251038.3:c.5507A>G	XP_005251095.1:p.Glu1836Gly
XM_005251040.3:c.5699A>G	XP_005251097.1:p.Glu1900Gly
XM_005251042.3:c.5699A>G	XP_005251099.1:p.Glu1900Gly
XM_005251043.3:c.5699A>G	XP_005251100.1:p.Glu1900Gly
XM_006716622.2:c.5699A>G	XP_006716685.1:p.Glu1900Gly
XM_005251038.4:c.5507A>G	XP_005251095.1:p.Glu1836Gly
XM_005251040.4:c.5699A>G	XP_005251097.1:p.Glu1900Gly
XM_005251042.4:c.5699A>G	XP_005251099.1:p.Glu1900Gly
XM_006716622.3:c.5699A>G	XP_006716685.1:p.Glu1900Gly
XM_017013793.1:c.5633A>G	XP_016869282.1:p.Glu1878Gly
XM_017013794.1:c.5699A>G	XP_016869283.1:p.Glu1900Gly
XM_017013795.1:c.5528A>G	XP_016869284.1:p.Glu1843Gly
XM_017013796.1:c.5480A>G	XP_016869285.1:p.Glu1827Gly
XM_017013797.1:c.5438A>G	XP_016869286.1:p.Glu1813Gly
XM_017013798.1:c.5699A>G	XP_016869287.1:p.Glu1900Gly
XM_017013799.1:c.5699A>G	XP_016869288.1:p.Glu1900Gly
XM_017013800.1:c.5699A>G	XP_016869289.1:p.Glu1900Gly
NM_003235.5:c.5699A>G MANE Select	NP_003226.4:p.Glu1900Gly