Canonical Allele Identifier: CA2576019288
Gene: TK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66513756del , CM000678.2:g.66513756del GRCh38
NC_000016.9:g.66547659del , CM000678.1:g.66547659del GRCh37
NC_000016.8:g.65105160del NCBI36
NG_016862.1:g.41660del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.509del ENSP00000299697.9:p.Phe170SerfsTer9
ENST00000417693.8:c.623del ENSP00000407469.5:p.Phe208SerfsTer9
ENST00000451102.7:c.584del ENSP00000414334.4:p.Phe195SerfsTer9
ENST00000527284.6:c.563-1687del
ENST00000527800.6:c.386del ENSP00000433770.1:p.Phe129SerfsTer9
ENST00000544898.6:c.677del MANE Select ENSP00000440898.2:p.Phe226SerfsTer9
ENST00000567357.6:c.*535del ENSP00000457959.2:n.*535del
ENST00000569718.6:c.415del ENSP00000464313.2:p.Ser139ProfsTer10
ENST00000620035.5:c.433del ENSP00000483833.2:p.Ser145ProfsTer10
ENST00000676538.1:c.260del
ENST00000676904.1:c.148del
ENST00000677296.1:n.59del
ENST00000677379.1:c.318del ENSP00000503672.1:n.318del
ENST00000677420.1:c.386del ENSP00000504648.1:p.Phe129SerfsTer9
ENST00000677555.1:c.386del ENSP00000503331.1:p.Phe129SerfsTer9
ENST00000677715.1:c.386del ENSP00000502950.1:p.Phe129SerfsTer9
ENST00000677753.1:n.59del
ENST00000677961.1:n.89del
ENST00000678015.1:c.386del ENSP00000502959.1:p.Phe129SerfsTer9
ENST00000678190.1:c.59del ENSP00000503824.1:p.Phe20SerfsTer?
ENST00000678282.1:n.59del
ENST00000678297.1:c.386del ENSP00000503472.1:p.Phe129SerfsTer9
ENST00000299697.11:c.677del ENSP00000299697.8:p.Phe226SerfsTer9
ENST00000417693.7:c.749del ENSP00000407469.4:p.Phe250SerfsTer9
ENST00000451102.6:c.803del ENSP00000414334.3:p.Phe268SerfsTer9
ENST00000525974.5:c.386del ENSP00000434594.1:p.Phe129SerfsTer9
ENST00000527284.5:c.584del ENSP00000435312.1:p.Phe195SerfsTer9
ENST00000527800.5:c.386del ENSP00000433770.1:p.Phe129SerfsTer9
ENST00000544898.5:c.677del ENSP00000440898.2:p.Phe226SerfsTer9
ENST00000545043.6:c.602del ENSP00000438143.2:p.Phe201SerfsTer9
ENST00000561527.5:n.236del
ENST00000561728.1:c.126del
ENST00000561905.2:c.31del
ENST00000562552.5:n.493del
ENST00000563099.5:n.204del
ENST00000563369.6:c.386del ENSP00000463560.1:p.Phe129SerfsTer9
ENST00000563478.5:c.386del ENSP00000462341.1:p.Phe129SerfsTer?
ENST00000564792.1:n.332del
ENST00000564917.5:c.728del ENSP00000455187.1:p.Phe243SerfsTer9
ENST00000567357.5:c.*535del ENSP00000457959.1:n.*535del
ENST00000569718.5:c.402del
ENST00000620035.4:c.623del ENSP00000483833.1:p.Phe208SerfsTer9
NM_001172643.1:c.584del NP_001166114.1:p.Phe195SerfsTer9
NM_001172644.1:c.602del NP_001166115.1:p.Phe201SerfsTer9
NM_001172645.1:c.623del NP_001166116.1:p.Phe208SerfsTer9
NM_001271934.1:c.530del NP_001258863.1:p.Phe177SerfsTer9
NM_001271935.1:c.415del NP_001258864.1:p.Ser139ProfsTer10
NM_001272050.1:c.386del NP_001258979.1:p.Phe129SerfsTer9
NM_004614.4:c.677del NP_004605.4:p.Phe226SerfsTer9
NR_073520.1:n.1956del
NM_001172644.2:c.602del NP_001166115.1:p.Phe201SerfsTer9
NM_001271934.2:c.530del NP_001258863.1:p.Phe177SerfsTer9
NM_001272050.2:c.386del NP_001258979.1:p.Phe129SerfsTer9
NM_004614.5:c.677del MANE Select NP_004605.4:p.Phe226SerfsTer9
NR_073520.2:n.1666del
NM_001172645.2:c.623del NP_001166116.1:p.Phe208SerfsTer9