Canonical Allele Identifier: CA2228911903
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66529058C= , CM000678.2:g.66529058C= GRCh38
NC_000016.9:g.66562961C= , CM000678.1:g.66562961C= GRCh37
NC_000016.8:g.65120462C= NCBI36
NG_016862.1:g.26355G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299697.12:c.217G= ENSP00000299697.9:p.Val73=
ENST00000417693.8:c.331G= ENSP00000407469.5:p.Val111=
ENST00000451102.7:c.292G= ENSP00000414334.4:p.Val98=
ENST00000527284.6:c.329G=
ENST00000527800.6:c.94G= ENSP00000433770.1:p.Val32=
ENST00000544898.6:c.385G= MANE Select ENSP00000440898.2:p.Val129=
ENST00000567357.6:c.*243G= ENSP00000457959.2:n.*243G=
ENST00000569718.6:c.292G= ENSP00000464313.2:p.Val98=
ENST00000620035.5:c.310G= ENSP00000483833.2:p.Val104=
ENST00000676538.1:c.33-11181G=
ENST00000677379.1:c.90+2322G= ENSP00000503672.1:n.90+2322G=
ENST00000677420.1:c.94G= ENSP00000504648.1:p.Val32=
ENST00000677555.1:c.94G= ENSP00000503331.1:p.Val32=
ENST00000677715.1:c.94G= ENSP00000502950.1:p.Val32=
ENST00000677739.1:c.64G= ENSP00000504644.1:p.Val22=
ENST00000678015.1:c.94G= ENSP00000502959.1:p.Val32=
ENST00000678297.1:c.94G= ENSP00000503472.1:p.Val32=
ENST00000678314.1:c.94G= ENSP00000504438.1:p.Val32=
ENST00000678746.1:c.275G= ENSP00000503227.1:n.275G=
ENST00000299697.11:c.385G= ENSP00000299697.8:p.Val129=
ENST00000417693.7:c.457G= ENSP00000407469.4:p.Val153=
ENST00000451102.6:c.511G= ENSP00000414334.3:p.Val171=
ENST00000525974.5:c.94G= ENSP00000434594.1:p.Val32=
ENST00000527284.5:c.292G= ENSP00000435312.1:p.Val98=
ENST00000527800.5:c.94G= ENSP00000433770.1:p.Val32=
ENST00000544898.5:c.385G= ENSP00000440898.2:p.Val129=
ENST00000545043.6:c.310G= ENSP00000438143.2:p.Val104=
ENST00000562484.2:c.94G= ENSP00000463326.1:p.Val32=
ENST00000563369.6:c.94G= ENSP00000463560.1:p.Val32=
ENST00000563478.5:c.94G= ENSP00000462341.1:p.Val32=
ENST00000564917.5:c.385G= ENSP00000455187.1:p.Val129=
ENST00000567357.5:c.*243G= ENSP00000457959.1:n.*243G=
ENST00000569718.5:c.279G=
ENST00000620035.4:c.331G= ENSP00000483833.1:p.Val111=
NM_001172643.1:c.292G= NP_001166114.1:p.Val98=
NM_001172644.1:c.310G= NP_001166115.1:p.Val104=
NM_001172645.1:c.331G= NP_001166116.1:p.Val111=
NM_001271934.1:c.238G= NP_001258863.1:p.Val80=
NM_001271935.1:c.292G= NP_001258864.1:p.Val98=
NM_001272050.1:c.94G= NP_001258979.1:p.Val32=
NM_004614.4:c.385G= NP_004605.4:p.Val129=
NR_073520.1:n.1664G=
NM_001172644.2:c.310G= NP_001166115.1:p.Val104=
NM_001271934.2:c.238G= NP_001258863.1:p.Val80=
NM_001272050.2:c.94G= NP_001258979.1:p.Val32=
NM_004614.5:c.385G= MANE Select NP_004605.4:p.Val129=
NR_073520.2:n.1374G=
NM_001172645.2:c.331G= NP_001166116.1:p.Val111=