Canonical Allele Identifier: CA2228922556
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66549019A= , CM000678.2:g.66549019A= GRCh38
NC_000016.9:g.66582922A= , CM000678.1:g.66582922A= GRCh37
NC_000016.8:g.65140423A= NCBI36
NG_016862.1:g.6394T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.32-10T= ENSP00000299697.9:n.32-10T=
ENST00000417693.8:c.125-10T= ENSP00000407469.5:n.125-10T=
ENST00000451102.7:c.32-10T= ENSP00000414334.4:n.32-10T=
ENST00000527284.6:c.69-10T=
ENST00000527800.6:c.-177T= ENSP00000433770.1:n.-177T=
ENST00000544898.6:c.125-10T= MANE Select ENSP00000440898.2:n.125-10T=
ENST00000567357.6:c.125-10T= ENSP00000457959.2:n.125-10T=
ENST00000569718.6:c.32-10T= ENSP00000464313.2:n.32-10T=
ENST00000620035.5:c.125-10T= ENSP00000483833.2:n.125-10T=
ENST00000677420.1:c.-123T= ENSP00000504648.1:n.-123T=
ENST00000677555.1:c.-102T= ENSP00000503331.1:n.-102T=
ENST00000677715.1:c.-167-10T= ENSP00000502950.1:n.-167-10T=
ENST00000678015.1:c.-167-10T= ENSP00000502959.1:n.-167-10T=
ENST00000678297.1:c.-92-10T= ENSP00000503472.1:n.-92-10T=
ENST00000678314.1:c.-61+2521T= ENSP00000504438.1:n.-61+2521T=
ENST00000679271.1:n.31-10T=
ENST00000679327.1:n.1086T=
ENST00000299697.11:c.125-10T= ENSP00000299697.8:n.125-10T=
ENST00000417693.7:c.251-10T= ENSP00000407469.4:n.251-10T=
ENST00000451102.6:c.251-10T= ENSP00000414334.3:n.251-10T=
ENST00000525974.5:c.-167-10T= ENSP00000434594.1:n.-167-10T=
ENST00000527284.5:c.32-10T= ENSP00000435312.1:n.32-10T=
ENST00000527800.5:c.-177T= ENSP00000433770.1:n.-177T=
ENST00000544898.5:c.125-10T= ENSP00000440898.2:n.125-10T=
ENST00000545043.6:c.125-10T= ENSP00000438143.2:n.125-10T=
ENST00000562484.2:c.-167-10T= ENSP00000463326.1:n.-167-10T=
ENST00000563369.6:c.-167-10T= ENSP00000463560.1:n.-167-10T=
ENST00000563478.5:c.-167-10T= ENSP00000462341.1:n.-167-10T=
ENST00000564917.5:c.125-10T= ENSP00000455187.1:n.125-10T=
ENST00000567357.5:c.251-10T= ENSP00000457959.1:n.251-10T=
ENST00000569718.5:c.19-10T=
ENST00000620035.4:c.125-10T= ENSP00000483833.1:n.125-10T=
NM_001172643.1:c.32-10T= NP_001166114.1:n.32-10T=
NM_001172644.1:c.125-10T= NP_001166115.1:n.125-10T=
NM_001172645.1:c.125-10T= NP_001166116.1:n.125-10T=
NM_001271934.1:c.-118-10T= NP_001258863.1:n.-118-10T=
NM_001271935.1:c.32-10T= NP_001258864.1:n.32-10T=
NM_001272050.1:c.-167-10T= NP_001258979.1:n.-167-10T=
NM_004614.4:c.125-10T= NP_004605.4:n.125-10T=
NR_073520.1:n.1394T=
NM_001172644.2:c.125-10T= NP_001166115.1:n.125-10T=
NM_001271934.2:c.-118-10T= NP_001258863.1:n.-118-10T=
NM_001272050.2:c.-167-10T= NP_001258979.1:n.-167-10T=
NM_004614.5:c.125-10T= MANE Select NP_004605.4:n.125-10T=
NR_073520.2:n.1104T=
NM_001172645.2:c.125-10T= NP_001166116.1:n.125-10T=