Canonical Allele Identifier: CA2228908931
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66513762C= , CM000678.2:g.66513762C= GRCh38
NC_000016.9:g.66547665C= , CM000678.1:g.66547665C= GRCh37
NC_000016.8:g.65105166C= NCBI36
NG_016862.1:g.41651G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.500G= ENSP00000299697.9:p.Gly167=
ENST00000417693.8:c.614G= ENSP00000407469.5:p.Gly205=
ENST00000451102.7:c.575G= ENSP00000414334.4:p.Gly192=
ENST00000527284.6:c.563-1696G=
ENST00000527800.6:c.377G= ENSP00000433770.1:p.Gly126=
ENST00000544898.6:c.668G= MANE Select ENSP00000440898.2:p.Gly223=
ENST00000567357.6:c.*526G= ENSP00000457959.2:n.*526G=
ENST00000569718.6:c.406G= ENSP00000464313.2:p.Ala136=
ENST00000620035.5:c.424G= ENSP00000483833.2:p.Ala142=
ENST00000676538.1:c.251G=
ENST00000676904.1:c.139G=
ENST00000677296.1:n.50G=
ENST00000677379.1:c.309G= ENSP00000503672.1:n.309G=
ENST00000677420.1:c.377G= ENSP00000504648.1:p.Gly126=
ENST00000677555.1:c.377G= ENSP00000503331.1:p.Gly126=
ENST00000677715.1:c.377G= ENSP00000502950.1:p.Gly126=
ENST00000677753.1:n.50G=
ENST00000677961.1:n.80G=
ENST00000678015.1:c.377G= ENSP00000502959.1:p.Gly126=
ENST00000678190.1:c.50G= ENSP00000503824.1:p.Gly17=
ENST00000678282.1:n.50G=
ENST00000678297.1:c.377G= ENSP00000503472.1:p.Gly126=
ENST00000299697.11:c.668G= ENSP00000299697.8:p.Gly223=
ENST00000417693.7:c.740G= ENSP00000407469.4:p.Gly247=
ENST00000451102.6:c.794G= ENSP00000414334.3:p.Gly265=
ENST00000525974.5:c.377G= ENSP00000434594.1:p.Gly126=
ENST00000527284.5:c.575G= ENSP00000435312.1:p.Gly192=
ENST00000527800.5:c.377G= ENSP00000433770.1:p.Gly126=
ENST00000544898.5:c.668G= ENSP00000440898.2:p.Gly223=
ENST00000545043.6:c.593G= ENSP00000438143.2:p.Gly198=
ENST00000561527.5:n.227G=
ENST00000561728.1:c.117G=
ENST00000561905.2:c.22G=
ENST00000562552.5:n.484G=
ENST00000563099.5:n.195G=
ENST00000563369.6:c.377G= ENSP00000463560.1:p.Gly126=
ENST00000563478.5:c.377G= ENSP00000462341.1:p.Gly126=
ENST00000564792.1:n.323G=
ENST00000564917.5:c.719G= ENSP00000455187.1:p.Gly240=
ENST00000567357.5:c.*526G= ENSP00000457959.1:n.*526G=
ENST00000569718.5:c.393G=
ENST00000620035.4:c.614G= ENSP00000483833.1:p.Gly205=
NM_001172643.1:c.575G= NP_001166114.1:p.Gly192=
NM_001172644.1:c.593G= NP_001166115.1:p.Gly198=
NM_001172645.1:c.614G= NP_001166116.1:p.Gly205=
NM_001271934.1:c.521G= NP_001258863.1:p.Gly174=
NM_001271935.1:c.406G= NP_001258864.1:p.Ala136=
NM_001272050.1:c.377G= NP_001258979.1:p.Gly126=
NM_004614.4:c.668G= NP_004605.4:p.Gly223=
NR_073520.1:n.1947G=
NM_001172644.2:c.593G= NP_001166115.1:p.Gly198=
NM_001271934.2:c.521G= NP_001258863.1:p.Gly174=
NM_001272050.2:c.377G= NP_001258979.1:p.Gly126=
NM_004614.5:c.668G= MANE Select NP_004605.4:p.Gly223=
NR_073520.2:n.1657G=
NM_001172645.2:c.614G= NP_001166116.1:p.Gly205=