Canonical Allele Identifier: CA2576019286
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66513737del , CM000678.2:g.66513737del GRCh38
NC_000016.9:g.66547640del , CM000678.1:g.66547640del GRCh37
NC_000016.8:g.65105141del NCBI36
NG_016862.1:g.41676del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.525del ENSP00000299697.9:p.Val176PhefsTer3
ENST00000417693.8:c.639del ENSP00000407469.5:p.Val214PhefsTer3
ENST00000451102.7:c.600del ENSP00000414334.4:p.Val201PhefsTer3
ENST00000527284.6:c.563-1671del
ENST00000527800.6:c.402del ENSP00000433770.1:p.Val135PhefsTer3
ENST00000544898.6:c.693del MANE Select ENSP00000440898.2:p.Val232PhefsTer3
ENST00000567357.6:c.*551del ENSP00000457959.2:n.*551del
ENST00000569718.6:c.431del ENSP00000464313.2:p.Leu144ArgfsTer5
ENST00000620035.5:c.449del ENSP00000483833.2:p.Leu150ArgfsTer5
ENST00000676538.1:c.276del
ENST00000676904.1:c.164del
ENST00000677296.1:n.75del
ENST00000677379.1:c.334del ENSP00000503672.1:n.334del
ENST00000677420.1:c.402del ENSP00000504648.1:p.Val135PhefsTer3
ENST00000677555.1:c.402del ENSP00000503331.1:p.Val135PhefsTer3
ENST00000677715.1:c.402del ENSP00000502950.1:p.Val135PhefsTer3
ENST00000677753.1:n.75del
ENST00000677961.1:n.105del
ENST00000678015.1:c.402del ENSP00000502959.1:p.Val135PhefsTer3
ENST00000678190.1:c.75del ENSP00000503824.1:p.Val26PhefsTer25
ENST00000678282.1:n.75del
ENST00000678297.1:c.402del ENSP00000503472.1:p.Val135PhefsTer3
ENST00000299697.11:c.693del ENSP00000299697.8:p.Val232PhefsTer3
ENST00000417693.7:c.765del ENSP00000407469.4:p.Val256PhefsTer3
ENST00000451102.6:c.819del ENSP00000414334.3:p.Val274PhefsTer3
ENST00000525974.5:c.402del ENSP00000434594.1:p.Val135PhefsTer3
ENST00000527284.5:c.600del ENSP00000435312.1:p.Val201PhefsTer3
ENST00000527800.5:c.402del ENSP00000433770.1:p.Val135PhefsTer3
ENST00000544898.5:c.693del ENSP00000440898.2:p.Val232PhefsTer3
ENST00000545043.6:c.618del ENSP00000438143.2:p.Val207PhefsTer3
ENST00000561527.5:n.252del
ENST00000561728.1:c.142del
ENST00000561905.2:c.47del
ENST00000562552.5:n.509del
ENST00000563099.5:n.220del
ENST00000563369.6:c.402del ENSP00000463560.1:p.Val135PhefsTer3
ENST00000564792.1:n.348del
ENST00000564917.5:c.744del ENSP00000455187.1:p.Val249PhefsTer3
ENST00000567357.5:c.*551del ENSP00000457959.1:n.*551del
ENST00000569718.5:c.418del
ENST00000620035.4:c.639del ENSP00000483833.1:p.Val214PhefsTer3
NM_001172643.1:c.600del NP_001166114.1:p.Val201PhefsTer3
NM_001172644.1:c.618del NP_001166115.1:p.Val207PhefsTer3
NM_001172645.1:c.639del NP_001166116.1:p.Val214PhefsTer3
NM_001271934.1:c.546del NP_001258863.1:p.Val183PhefsTer3
NM_001271935.1:c.431del NP_001258864.1:p.Leu144ArgfsTer5
NM_001272050.1:c.402del NP_001258979.1:p.Val135PhefsTer3
NM_004614.4:c.693del NP_004605.4:p.Val232PhefsTer3
NR_073520.1:n.1972del
NM_001172644.2:c.618del NP_001166115.1:p.Val207PhefsTer3
NM_001271934.2:c.546del NP_001258863.1:p.Val183PhefsTer3
NM_001272050.2:c.402del NP_001258979.1:p.Val135PhefsTer3
NM_004614.5:c.693del MANE Select NP_004605.4:p.Val232PhefsTer3
NR_073520.2:n.1682del
NM_001172645.2:c.639del NP_001166116.1:p.Val214PhefsTer3