Canonical Allele Identifier: CA323868
Gene: TK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66549968G>A , CM000678.2:g.66549968G>A GRCh38
NC_000016.9:g.66583871G>A , CM000678.1:g.66583871G>A GRCh37
NC_000016.8:g.65141372G>A NCBI36
NG_016862.1:g.5445C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.31+285C>T ENSP00000299697.9:n.31+285C>T
ENST00000417693.8:c.94C>T ENSP00000407469.5:p.Arg32Trp
ENST00000451102.7:c.31+285C>T ENSP00000414334.4:n.31+285C>T
ENST00000527284.6:c.38C>T
ENST00000544898.6:c.94C>T MANE Select ENSP00000440898.2:p.Arg32Trp
ENST00000567357.6:c.94C>T ENSP00000457959.2:p.Arg32Trp
ENST00000569718.6:c.31+285C>T ENSP00000464313.2:n.31+285C>T
ENST00000620035.5:c.94C>T ENSP00000483833.2:p.Arg32Trp
ENST00000677420.1:c.-1072C>T ENSP00000504648.1:n.-1072C>T
ENST00000678015.1:c.-167-959C>T ENSP00000502959.1:n.-167-959C>T
ENST00000678297.1:c.-92-959C>T ENSP00000503472.1:n.-92-959C>T
ENST00000678314.1:c.-61+1572C>T ENSP00000504438.1:n.-61+1572C>T
ENST00000679327.1:n.137C>T
ENST00000299697.11:c.94C>T ENSP00000299697.8:p.Arg32Trp
ENST00000417693.7:c.220C>T ENSP00000407469.4:p.Arg74Trp
ENST00000451102.6:c.220C>T ENSP00000414334.3:p.Arg74Trp
ENST00000527284.5:c.31+285C>T ENSP00000435312.1:n.31+285C>T
ENST00000544898.5:c.94C>T ENSP00000440898.2:p.Arg32Trp
ENST00000545043.6:c.94C>T ENSP00000438143.2:p.Arg32Trp
ENST00000562484.2:c.-167-959C>T ENSP00000463326.1:n.-167-959C>T
ENST00000563478.5:c.-167-959C>T ENSP00000462341.1:n.-167-959C>T
ENST00000564917.5:c.94C>T ENSP00000455187.1:p.Arg32Trp
ENST00000567357.5:c.220C>T ENSP00000457959.1:p.Arg74Trp
ENST00000569718.5:c.18+285C>T
ENST00000620035.4:c.94C>T ENSP00000483833.1:p.Arg32Trp
NM_001172643.1:c.31+285C>T NP_001166114.1:n.31+285C>T
NM_001172644.1:c.94C>T NP_001166115.1:p.Arg32Trp
NM_001172645.1:c.94C>T NP_001166116.1:p.Arg32Trp
NM_001271934.1:c.-149C>T NP_001258863.1:n.-149C>T
NM_001271935.1:c.31+285C>T NP_001258864.1:n.31+285C>T
NM_004614.4:c.94C>T NP_004605.4:p.Arg32Trp
NR_073520.1:n.445C>T
NM_001172644.2:c.94C>T NP_001166115.1:p.Arg32Trp
NM_001271934.2:c.-149C>T NP_001258863.1:n.-149C>T
NM_001272050.2:c.-559C>T NP_001258979.1:n.-559C>T
NM_004614.5:c.94C>T MANE Select NP_004605.4:p.Arg32Trp
NR_073520.2:n.155C>T
NM_001172645.2:c.94C>T NP_001166116.1:p.Arg32Trp