Canonical Allele Identifier: CA2228912983
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66531441C= , CM000678.2:g.66531441C= GRCh38
NC_000016.9:g.66565344C= , CM000678.1:g.66565344C= GRCh37
NC_000016.8:g.65122845C= NCBI36
NG_016862.1:g.23972G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299697.12:c.146G= ENSP00000299697.9:p.Trp49=
ENST00000417693.8:c.260G= ENSP00000407469.5:p.Trp87=
ENST00000451102.7:c.221G= ENSP00000414334.4:p.Trp74=
ENST00000527284.6:c.258G=
ENST00000527800.6:c.23G= ENSP00000433770.1:p.Trp8=
ENST00000544898.6:c.314G= MANE Select ENSP00000440898.2:p.Trp105=
ENST00000567357.6:c.*172G= ENSP00000457959.2:n.*172G=
ENST00000569718.6:c.221G= ENSP00000464313.2:p.Trp74=
ENST00000620035.5:c.239G= ENSP00000483833.2:p.Trp80=
ENST00000676538.1:c.33-13564G=
ENST00000677379.1:c.29G= ENSP00000503672.1:p.Trp10=
ENST00000677420.1:c.23G= ENSP00000504648.1:p.Trp8=
ENST00000677497.1:n.201G=
ENST00000677555.1:c.23G= ENSP00000503331.1:p.Trp8=
ENST00000677715.1:c.23G= ENSP00000502950.1:p.Trp8=
ENST00000677739.1:c.55-2374G= ENSP00000504644.1:n.55-2374G=
ENST00000678015.1:c.23G= ENSP00000502959.1:p.Trp8=
ENST00000678297.1:c.23G= ENSP00000503472.1:p.Trp8=
ENST00000678314.1:c.23G= ENSP00000504438.1:p.Trp8=
ENST00000678746.1:c.204G= ENSP00000503227.1:n.204G=
ENST00000679154.1:c.61G=
ENST00000299697.11:c.314G= ENSP00000299697.8:p.Trp105=
ENST00000417693.7:c.386G= ENSP00000407469.4:p.Trp129=
ENST00000451102.6:c.440G= ENSP00000414334.3:p.Trp147=
ENST00000525974.5:c.23G= ENSP00000434594.1:p.Trp8=
ENST00000527284.5:c.221G= ENSP00000435312.1:p.Trp74=
ENST00000527800.5:c.23G= ENSP00000433770.1:p.Trp8=
ENST00000544898.5:c.314G= ENSP00000440898.2:p.Trp105=
ENST00000545043.6:c.239G= ENSP00000438143.2:p.Trp80=
ENST00000562484.2:c.23G= ENSP00000463326.1:p.Trp8=
ENST00000563369.6:c.23G= ENSP00000463560.1:p.Trp8=
ENST00000563478.5:c.23G= ENSP00000462341.1:p.Trp8=
ENST00000564917.5:c.314G= ENSP00000455187.1:p.Trp105=
ENST00000567357.5:c.*172G= ENSP00000457959.1:n.*172G=
ENST00000569718.5:c.208G=
ENST00000620035.4:c.260G= ENSP00000483833.1:p.Trp87=
NM_001172643.1:c.221G= NP_001166114.1:p.Trp74=
NM_001172644.1:c.239G= NP_001166115.1:p.Trp80=
NM_001172645.1:c.260G= NP_001166116.1:p.Trp87=
NM_001271934.1:c.167G= NP_001258863.1:p.Trp56=
NM_001271935.1:c.221G= NP_001258864.1:p.Trp74=
NM_001272050.1:c.23G= NP_001258979.1:p.Trp8=
NM_004614.4:c.314G= NP_004605.4:p.Trp105=
NR_073520.1:n.1593G=
NM_001172644.2:c.239G= NP_001166115.1:p.Trp80=
NM_001271934.2:c.167G= NP_001258863.1:p.Trp56=
NM_001272050.2:c.23G= NP_001258979.1:p.Trp8=
NM_004614.5:c.314G= MANE Select NP_004605.4:p.Trp105=
NR_073520.2:n.1303G=
NM_001172645.2:c.260G= NP_001166116.1:p.Trp87=