Canonical Allele Identifier: CA2228896306
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66513783T= , CM000678.2:g.66513783T= GRCh38
NC_000016.9:g.66547686T= , CM000678.1:g.66547686T= GRCh37
NC_000016.8:g.65105187T= NCBI36
NG_016862.1:g.41630A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.479A= ENSP00000299697.9:p.His160=
ENST00000417693.8:c.593A= ENSP00000407469.5:p.His198=
ENST00000451102.7:c.554A= ENSP00000414334.4:p.His185=
ENST00000527284.6:c.563-1717A=
ENST00000527800.6:c.356A= ENSP00000433770.1:p.His119=
ENST00000544898.6:c.647A= MANE Select ENSP00000440898.2:p.His216=
ENST00000567357.6:c.*505A= ENSP00000457959.2:n.*505A=
ENST00000569718.6:c.385A= ENSP00000464313.2:p.Met129=
ENST00000620035.5:c.403A= ENSP00000483833.2:p.Met135=
ENST00000676538.1:c.230A=
ENST00000676904.1:c.118A=
ENST00000677296.1:n.29A=
ENST00000677379.1:c.288A= ENSP00000503672.1:n.288A=
ENST00000677420.1:c.356A= ENSP00000504648.1:p.His119=
ENST00000677555.1:c.356A= ENSP00000503331.1:p.His119=
ENST00000677715.1:c.356A= ENSP00000502950.1:p.His119=
ENST00000677753.1:n.29A=
ENST00000677961.1:n.59A=
ENST00000678015.1:c.356A= ENSP00000502959.1:p.His119=
ENST00000678190.1:c.29A= ENSP00000503824.1:p.His10=
ENST00000678282.1:n.29A=
ENST00000678297.1:c.356A= ENSP00000503472.1:p.His119=
ENST00000299697.11:c.647A= ENSP00000299697.8:p.His216=
ENST00000417693.7:c.719A= ENSP00000407469.4:p.His240=
ENST00000451102.6:c.773A= ENSP00000414334.3:p.His258=
ENST00000525974.5:c.356A= ENSP00000434594.1:p.His119=
ENST00000527284.5:c.554A= ENSP00000435312.1:p.His185=
ENST00000527800.5:c.356A= ENSP00000433770.1:p.His119=
ENST00000544898.5:c.647A= ENSP00000440898.2:p.His216=
ENST00000545043.6:c.572A= ENSP00000438143.2:p.His191=
ENST00000561527.5:n.206A=
ENST00000561728.1:c.96A=
ENST00000561905.2:c.1A=
ENST00000562552.5:n.463A=
ENST00000563099.5:n.174A=
ENST00000563369.6:c.356A= ENSP00000463560.1:p.His119=
ENST00000563478.5:c.356A= ENSP00000462341.1:p.His119=
ENST00000564792.1:n.302A=
ENST00000564917.5:c.698A= ENSP00000455187.1:p.His233=
ENST00000567357.5:c.*505A= ENSP00000457959.1:n.*505A=
ENST00000569718.5:c.372A=
ENST00000620035.4:c.593A= ENSP00000483833.1:p.His198=
NM_001172643.1:c.554A= NP_001166114.1:p.His185=
NM_001172644.1:c.572A= NP_001166115.1:p.His191=
NM_001172645.1:c.593A= NP_001166116.1:p.His198=
NM_001271934.1:c.500A= NP_001258863.1:p.His167=
NM_001271935.1:c.385A= NP_001258864.1:p.Met129=
NM_001272050.1:c.356A= NP_001258979.1:p.His119=
NM_004614.4:c.647A= NP_004605.4:p.His216=
NR_073520.1:n.1926A=
NM_001172644.2:c.572A= NP_001166115.1:p.His191=
NM_001271934.2:c.500A= NP_001258863.1:p.His167=
NM_001272050.2:c.356A= NP_001258979.1:p.His119=
NM_004614.5:c.647A= MANE Select NP_004605.4:p.His216=
NR_073520.2:n.1636A=
NM_001172645.2:c.593A= NP_001166116.1:p.His198=