Canonical Allele Identifier: CA372236661

Gene: TG

Linked Data

• COSMIC: COSM254981
• MyVariant Identifiers: chr8:g.133984072C>A (hg19) ; chr8:g.132971827C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971827C>A , CM000670.2:g.132971827C>A	GRCh38
NC_000008.10:g.133984072C>A , CM000670.1:g.133984072C>A	GRCh37
NC_000008.9:g.134053254C>A	NCBI36
NG_015832.1:g.109868C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6009C>A MANE Select	ENSP00000220616.4:p.Asp2003Glu
ENST00000220616.8:c.6009C>A	ENSP00000220616.4:p.Asp2003Glu
ENST00000519178.5:c.1375C>A
ENST00000519294.5:n.1C>A
ENST00000519543.5:c.471C>A	ENSP00000430430.1:p.Asp157Glu
ENST00000520089.5:n.118C>A
ENST00000520197.5:n.146C>A
ENST00000523756.5:c.2664C>A
NM_003235.4:c.6009C>A	NP_003226.4:p.Asp2003Glu
XM_005251038.3:c.5817C>A	XP_005251095.1:p.Asp1939Glu
XM_005251040.3:c.6009C>A	XP_005251097.1:p.Asp2003Glu
XM_005251042.3:c.6009C>A	XP_005251099.1:p.Asp2003Glu
XM_005251043.3:c.6009C>A	XP_005251100.1:p.Asp2003Glu
XM_006716622.2:c.6009C>A	XP_006716685.1:p.Asp2003Glu
XM_005251038.4:c.5817C>A	XP_005251095.1:p.Asp1939Glu
XM_005251040.4:c.6009C>A	XP_005251097.1:p.Asp2003Glu
XM_005251042.4:c.6009C>A	XP_005251099.1:p.Asp2003Glu
XM_006716622.3:c.6009C>A	XP_006716685.1:p.Asp2003Glu
XM_017013793.1:c.5943C>A	XP_016869282.1:p.Asp1981Glu
XM_017013794.1:c.6009C>A	XP_016869283.1:p.Asp2003Glu
XM_017013795.1:c.5838C>A	XP_016869284.1:p.Asp1946Glu
XM_017013796.1:c.5790C>A	XP_016869285.1:p.Asp1930Glu
XM_017013797.1:c.5748C>A	XP_016869286.1:p.Asp1916Glu
XM_017013798.1:c.6009C>A	XP_016869287.1:p.Asp2003Glu
XM_017013799.1:c.6009C>A	XP_016869288.1:p.Asp2003Glu
XM_017013800.1:c.6009C>A	XP_016869289.1:p.Asp2003Glu
NM_003235.5:c.6009C>A MANE Select	NP_003226.4:p.Asp2003Glu