Canonical Allele Identifier: CA2228912985
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66531444C= , CM000678.2:g.66531444C= GRCh38
NC_000016.9:g.66565347C= , CM000678.1:g.66565347C= GRCh37
NC_000016.8:g.65122848C= NCBI36
NG_016862.1:g.23969G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299697.12:c.143G= ENSP00000299697.9:p.Arg48=
ENST00000417693.8:c.257G= ENSP00000407469.5:p.Arg86=
ENST00000451102.7:c.218G= ENSP00000414334.4:p.Arg73=
ENST00000527284.6:c.255G=
ENST00000527800.6:c.20G= ENSP00000433770.1:p.Arg7=
ENST00000544898.6:c.311G= MANE Select ENSP00000440898.2:p.Arg104=
ENST00000567357.6:c.*169G= ENSP00000457959.2:n.*169G=
ENST00000569718.6:c.218G= ENSP00000464313.2:p.Arg73=
ENST00000620035.5:c.236G= ENSP00000483833.2:p.Arg79=
ENST00000676538.1:c.33-13567G=
ENST00000677379.1:c.26G= ENSP00000503672.1:p.Arg9=
ENST00000677420.1:c.20G= ENSP00000504648.1:p.Arg7=
ENST00000677497.1:n.198G=
ENST00000677555.1:c.20G= ENSP00000503331.1:p.Arg7=
ENST00000677715.1:c.20G= ENSP00000502950.1:p.Arg7=
ENST00000677739.1:c.55-2377G= ENSP00000504644.1:n.55-2377G=
ENST00000678015.1:c.20G= ENSP00000502959.1:p.Arg7=
ENST00000678297.1:c.20G= ENSP00000503472.1:p.Arg7=
ENST00000678314.1:c.20G= ENSP00000504438.1:p.Arg7=
ENST00000678746.1:c.201G= ENSP00000503227.1:n.201G=
ENST00000679154.1:c.58G=
ENST00000299697.11:c.311G= ENSP00000299697.8:p.Arg104=
ENST00000417693.7:c.383G= ENSP00000407469.4:p.Arg128=
ENST00000451102.6:c.437G= ENSP00000414334.3:p.Arg146=
ENST00000525974.5:c.20G= ENSP00000434594.1:p.Arg7=
ENST00000527284.5:c.218G= ENSP00000435312.1:p.Arg73=
ENST00000527800.5:c.20G= ENSP00000433770.1:p.Arg7=
ENST00000544898.5:c.311G= ENSP00000440898.2:p.Arg104=
ENST00000545043.6:c.236G= ENSP00000438143.2:p.Arg79=
ENST00000562484.2:c.20G= ENSP00000463326.1:p.Arg7=
ENST00000563369.6:c.20G= ENSP00000463560.1:p.Arg7=
ENST00000563478.5:c.20G= ENSP00000462341.1:p.Arg7=
ENST00000564917.5:c.311G= ENSP00000455187.1:p.Arg104=
ENST00000567357.5:c.*169G= ENSP00000457959.1:n.*169G=
ENST00000569718.5:c.205G=
ENST00000620035.4:c.257G= ENSP00000483833.1:p.Arg86=
NM_001172643.1:c.218G= NP_001166114.1:p.Arg73=
NM_001172644.1:c.236G= NP_001166115.1:p.Arg79=
NM_001172645.1:c.257G= NP_001166116.1:p.Arg86=
NM_001271934.1:c.164G= NP_001258863.1:p.Arg55=
NM_001271935.1:c.218G= NP_001258864.1:p.Arg73=
NM_001272050.1:c.20G= NP_001258979.1:p.Arg7=
NM_004614.4:c.311G= NP_004605.4:p.Arg104=
NR_073520.1:n.1590G=
NM_001172644.2:c.236G= NP_001166115.1:p.Arg79=
NM_001271934.2:c.164G= NP_001258863.1:p.Arg55=
NM_001272050.2:c.20G= NP_001258979.1:p.Arg7=
NM_004614.5:c.311G= MANE Select NP_004605.4:p.Arg104=
NR_073520.2:n.1300G=
NM_001172645.2:c.257G= NP_001166116.1:p.Arg86=