Canonical Allele Identifier: CA343296
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66541893_66541894dup , CM000678.2:g.66541893_66541894dup GRCh38
NC_000016.9:g.66575796_66575797dup , CM000678.1:g.66575796_66575797dup GRCh37
NC_000016.8:g.65133297_65133298dup NCBI36
NG_016862.1:g.13521_13522dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.64-4875_64-4874dup ENSP00000299697.9:n.64-4875_64-4874dup
ENST00000417693.8:c.218_219dup ENSP00000407469.5:p.Thr74ArgfsTer7
ENST00000451102.7:c.125_126dup ENSP00000414334.4:p.Thr43ArgfsTer7
ENST00000527284.6:c.162_163dup
ENST00000527800.6:c.-74_-73dup ENSP00000433770.1:n.-74_-73dup
ENST00000544898.6:c.218_219dup MANE Select ENSP00000440898.2:p.Thr74ArgfsTer7
ENST00000567357.6:c.*76_*77dup ENSP00000457959.2:n.*76_*77dup
ENST00000569718.6:c.125_126dup ENSP00000464313.2:p.Thr43ArgfsTer7
ENST00000620035.5:c.157-4875_157-4874dup ENSP00000483833.2:n.157-4875_157-4874dup
ENST00000676536.1:c.174_175dup
ENST00000676538.1:c.32+7086_32+7087dup
ENST00000677412.1:c.169_170dup
ENST00000677420.1:c.-20_-19dup ENSP00000504648.1:n.-20_-19dup
ENST00000677541.1:c.211_212dup
ENST00000677555.1:c.-60-4875_-60-4874dup ENSP00000503331.1:n.-60-4875_-60-4874dup
ENST00000677715.1:c.-74_-73dup ENSP00000502950.1:n.-74_-73dup
ENST00000678015.1:c.-74_-73dup ENSP00000502959.1:n.-74_-73dup
ENST00000678205.1:c.231_232dup
ENST00000678297.1:c.-60-4875_-60-4874dup ENSP00000503472.1:n.-60-4875_-60-4874dup
ENST00000678314.1:c.-60-4875_-60-4874dup ENSP00000504438.1:n.-60-4875_-60-4874dup
ENST00000678336.1:n.205_206dup
ENST00000678864.1:n.96-4875_96-4874dup
ENST00000679154.1:c.32+7086_32+7087dup
ENST00000679327.1:n.1189_1190dup
ENST00000299697.11:c.218_219dup ENSP00000299697.8:p.Thr74ArgfsTer7
ENST00000417693.7:c.344_345dup ENSP00000407469.4:p.Thr116ArgfsTer7
ENST00000451102.6:c.344_345dup ENSP00000414334.3:p.Thr116ArgfsTer7
ENST00000525974.5:c.-74_-73dup ENSP00000434594.1:n.-74_-73dup
ENST00000527284.5:c.125_126dup ENSP00000435312.1:p.Thr43ArgfsTer7
ENST00000527800.5:c.-74_-73dup ENSP00000433770.1:n.-74_-73dup
ENST00000544898.5:c.218_219dup ENSP00000440898.2:p.Thr74ArgfsTer7
ENST00000545043.6:c.157-4875_157-4874dup ENSP00000438143.2:n.157-4875_157-4874dup
ENST00000562484.2:c.-74_-73dup ENSP00000463326.1:n.-74_-73dup
ENST00000563369.6:c.-74_-73dup ENSP00000463560.1:n.-74_-73dup
ENST00000563478.5:c.-74_-73dup ENSP00000462341.1:n.-74_-73dup
ENST00000564917.5:c.218_219dup ENSP00000455187.1:p.Thr74ArgfsTer7
ENST00000567357.5:c.*76_*77dup ENSP00000457959.1:n.*76_*77dup
ENST00000569718.5:c.112_113dup
ENST00000620035.4:c.218_219dup ENSP00000483833.1:p.Thr74ArgfsTer7
NM_001172643.1:c.125_126dup NP_001166114.1:p.Thr43ArgfsTer7
NM_001172644.1:c.157-4875_157-4874dup NP_001166115.1:n.157-4875_157-4874dup
NM_001172645.1:c.218_219dup NP_001166116.1:p.Thr74ArgfsTer7
NM_001271934.1:c.71_72dup NP_001258863.1:p.Thr25ArgfsTer7
NM_001271935.1:c.125_126dup NP_001258864.1:p.Thr43ArgfsTer7
NM_001272050.1:c.-74_-73dup NP_001258979.1:n.-74_-73dup
NM_004614.4:c.218_219dup NP_004605.4:p.Thr74ArgfsTer7
NR_073520.1:n.1497_1498dup
NM_001172644.2:c.157-4875_157-4874dup NP_001166115.1:n.157-4875_157-4874dup
NM_001271934.2:c.71_72dup NP_001258863.1:p.Thr25ArgfsTer7
NM_001272050.2:c.-74_-73dup NP_001258979.1:n.-74_-73dup
NM_004614.5:c.218_219dup MANE Select NP_004605.4:p.Thr74ArgfsTer7
NR_073520.2:n.1207_1208dup
NM_001172645.2:c.218_219dup NP_001166116.1:p.Thr74ArgfsTer7