Canonical Allele Identifier: CA396193343
Gene: TK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66549004C>A , CM000678.2:g.66549004C>A GRCh38
NC_000016.9:g.66582907C>A , CM000678.1:g.66582907C>A GRCh37
NC_000016.8:g.65140408C>A NCBI36
NG_016862.1:g.6409G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.37G>T ENSP00000299697.9:p.Glu13Ter
ENST00000417693.8:c.130G>T ENSP00000407469.5:p.Glu44Ter
ENST00000451102.7:c.37G>T ENSP00000414334.4:p.Glu13Ter
ENST00000527284.6:c.74G>T
ENST00000527800.6:c.-162G>T ENSP00000433770.1:n.-162G>T
ENST00000544898.6:c.130G>T MANE Select ENSP00000440898.2:p.Glu44Ter
ENST00000567357.6:c.130G>T ENSP00000457959.2:p.Glu44Ter
ENST00000569718.6:c.37G>T ENSP00000464313.2:p.Glu13Ter
ENST00000620035.5:c.130G>T ENSP00000483833.2:p.Glu44Ter
ENST00000676536.1:c.6G>T
ENST00000676538.1:c.6G>T
ENST00000677124.1:n.6G>T
ENST00000677412.1:c.6G>T
ENST00000677420.1:c.-108G>T ENSP00000504648.1:n.-108G>T
ENST00000677541.1:c.6G>T
ENST00000677555.1:c.-87G>T ENSP00000503331.1:n.-87G>T
ENST00000677715.1:c.-162G>T ENSP00000502950.1:n.-162G>T
ENST00000678015.1:c.-162G>T ENSP00000502959.1:n.-162G>T
ENST00000678205.1:c.6G>T
ENST00000678297.1:c.-87G>T ENSP00000503472.1:n.-87G>T
ENST00000678314.1:c.-61+2536G>T ENSP00000504438.1:n.-61+2536G>T
ENST00000679154.1:c.6G>T
ENST00000679271.1:n.36G>T
ENST00000679327.1:n.1101G>T
ENST00000299697.11:c.130G>T ENSP00000299697.8:p.Glu44Ter
ENST00000417693.7:c.256G>T ENSP00000407469.4:p.Glu86Ter
ENST00000451102.6:c.256G>T ENSP00000414334.3:p.Glu86Ter
ENST00000525974.5:c.-162G>T ENSP00000434594.1:n.-162G>T
ENST00000527284.5:c.37G>T ENSP00000435312.1:p.Glu13Ter
ENST00000527800.5:c.-162G>T ENSP00000433770.1:n.-162G>T
ENST00000544898.5:c.130G>T ENSP00000440898.2:p.Glu44Ter
ENST00000545043.6:c.130G>T ENSP00000438143.2:p.Glu44Ter
ENST00000562484.2:c.-162G>T ENSP00000463326.1:n.-162G>T
ENST00000563369.6:c.-162G>T ENSP00000463560.1:n.-162G>T
ENST00000563478.5:c.-162G>T ENSP00000462341.1:n.-162G>T
ENST00000564917.5:c.130G>T ENSP00000455187.1:p.Glu44Ter
ENST00000567357.5:c.256G>T ENSP00000457959.1:p.Glu86Ter
ENST00000569718.5:c.24G>T
ENST00000620035.4:c.130G>T ENSP00000483833.1:p.Glu44Ter
NM_001172643.1:c.37G>T NP_001166114.1:p.Glu13Ter
NM_001172644.1:c.130G>T NP_001166115.1:p.Glu44Ter
NM_001172645.1:c.130G>T NP_001166116.1:p.Glu44Ter
NM_001271934.1:c.-113G>T NP_001258863.1:n.-113G>T
NM_001271935.1:c.37G>T NP_001258864.1:p.Glu13Ter
NM_001272050.1:c.-162G>T NP_001258979.1:n.-162G>T
NM_004614.4:c.130G>T NP_004605.4:p.Glu44Ter
NR_073520.1:n.1409G>T
NM_001172644.2:c.130G>T NP_001166115.1:p.Glu44Ter
NM_001271934.2:c.-113G>T NP_001258863.1:n.-113G>T
NM_001272050.2:c.-162G>T NP_001258979.1:n.-162G>T
NM_004614.5:c.130G>T MANE Select NP_004605.4:p.Glu44Ter
NR_073520.2:n.1119G>T
NM_001172645.2:c.130G>T NP_001166116.1:p.Glu44Ter