Canonical Allele Identifier: CA2576019287
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66513741del , CM000678.2:g.66513741del GRCh38
NC_000016.9:g.66547644del , CM000678.1:g.66547644del GRCh37
NC_000016.8:g.65105145del NCBI36
NG_016862.1:g.41675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.524del ENSP00000299697.9:p.Pro175LeufsTer4
ENST00000417693.8:c.638del ENSP00000407469.5:p.Pro213LeufsTer4
ENST00000451102.7:c.599del ENSP00000414334.4:p.Pro200LeufsTer4
ENST00000527284.6:c.563-1672del
ENST00000527800.6:c.401del ENSP00000433770.1:p.Pro134LeufsTer4
ENST00000544898.6:c.692del MANE Select ENSP00000440898.2:p.Pro231LeufsTer4
ENST00000567357.6:c.*550del ENSP00000457959.2:n.*550del
ENST00000569718.6:c.430del ENSP00000464313.2:p.Leu144CysfsTer5
ENST00000620035.5:c.448del ENSP00000483833.2:p.Leu150CysfsTer5
ENST00000676538.1:c.275del
ENST00000676904.1:c.163del
ENST00000677296.1:n.74del
ENST00000677379.1:c.333del ENSP00000503672.1:n.333del
ENST00000677420.1:c.401del ENSP00000504648.1:p.Pro134LeufsTer4
ENST00000677555.1:c.401del ENSP00000503331.1:p.Pro134LeufsTer4
ENST00000677715.1:c.401del ENSP00000502950.1:p.Pro134LeufsTer4
ENST00000677753.1:n.74del
ENST00000677961.1:n.104del
ENST00000678015.1:c.401del ENSP00000502959.1:p.Pro134LeufsTer4
ENST00000678190.1:c.74del ENSP00000503824.1:p.Pro25LeufsTer26
ENST00000678282.1:n.74del
ENST00000678297.1:c.401del ENSP00000503472.1:p.Pro134LeufsTer4
ENST00000299697.11:c.692del ENSP00000299697.8:p.Pro231LeufsTer4
ENST00000417693.7:c.764del ENSP00000407469.4:p.Pro255LeufsTer4
ENST00000451102.6:c.818del ENSP00000414334.3:p.Pro273LeufsTer4
ENST00000525974.5:c.401del ENSP00000434594.1:p.Pro134LeufsTer4
ENST00000527284.5:c.599del ENSP00000435312.1:p.Pro200LeufsTer4
ENST00000527800.5:c.401del ENSP00000433770.1:p.Pro134LeufsTer4
ENST00000544898.5:c.692del ENSP00000440898.2:p.Pro231LeufsTer4
ENST00000545043.6:c.617del ENSP00000438143.2:p.Pro206LeufsTer4
ENST00000561527.5:n.251del
ENST00000561728.1:c.141del
ENST00000561905.2:c.46del
ENST00000562552.5:n.508del
ENST00000563099.5:n.219del
ENST00000563369.6:c.401del ENSP00000463560.1:p.Pro134LeufsTer4
ENST00000564792.1:n.347del
ENST00000564917.5:c.743del ENSP00000455187.1:p.Pro248LeufsTer4
ENST00000567357.5:c.*550del ENSP00000457959.1:n.*550del
ENST00000569718.5:c.417del
ENST00000620035.4:c.638del ENSP00000483833.1:p.Pro213LeufsTer4
NM_001172643.1:c.599del NP_001166114.1:p.Pro200LeufsTer4
NM_001172644.1:c.617del NP_001166115.1:p.Pro206LeufsTer4
NM_001172645.1:c.638del NP_001166116.1:p.Pro213LeufsTer4
NM_001271934.1:c.545del NP_001258863.1:p.Pro182LeufsTer4
NM_001271935.1:c.430del NP_001258864.1:p.Leu144CysfsTer5
NM_001272050.1:c.401del NP_001258979.1:p.Pro134LeufsTer4
NM_004614.4:c.692del NP_004605.4:p.Pro231LeufsTer4
NR_073520.1:n.1971del
NM_001172644.2:c.617del NP_001166115.1:p.Pro206LeufsTer4
NM_001271934.2:c.545del NP_001258863.1:p.Pro182LeufsTer4
NM_001272050.2:c.401del NP_001258979.1:p.Pro134LeufsTer4
NM_004614.5:c.692del MANE Select NP_004605.4:p.Pro231LeufsTer4
NR_073520.2:n.1681del
NM_001172645.2:c.638del NP_001166116.1:p.Pro213LeufsTer4