Canonical Allele Identifier: CA282171918

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66511745C>T , CM000678.2:g.66511745C>T	GRCh38
NC_000016.9:g.66545648C>T , CM000678.1:g.66545648C>T	GRCh37
NC_000016.8:g.65103149C>T	NCBI36
NG_016862.1:g.43668G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.*223G>A	ENSP00000299697.9:n.*223G>A
ENST00000451102.7:c.*223G>A	ENSP00000414334.4:n.*223G>A
ENST00000527284.6:c.884G>A
ENST00000527800.6:c.*223G>A	ENSP00000433770.1:n.*223G>A
ENST00000544898.6:c.*223G>A MANE Select	ENSP00000440898.2:n.*223G>A
ENST00000567357.6:c.*879G>A	ENSP00000457959.2:n.*879G>A
ENST00000569718.6:c.*318G>A	ENSP00000464313.2:n.*318G>A
ENST00000620035.5:c.*318G>A	ENSP00000483833.2:n.*318G>A
ENST00000677166.1:n.109+213G>A
ENST00000677319.1:c.109+213G>A	ENSP00000503900.1:n.109+213G>A
ENST00000677420.1:c.*223G>A	ENSP00000504648.1:n.*223G>A
ENST00000677535.1:c.322G>A	ENSP00000502856.1:n.322G>A
ENST00000677555.1:c.*223G>A	ENSP00000503331.1:n.*223G>A
ENST00000677753.1:n.81+1986G>A
ENST00000678015.1:c.*223G>A	ENSP00000502959.1:n.*223G>A
ENST00000678099.1:c.322G>A	ENSP00000504701.1:n.322G>A
ENST00000678190.1:c.469G>A	ENSP00000503824.1:n.469G>A
ENST00000678219.1:c.322G>A	ENSP00000504142.1:n.322G>A
ENST00000678282.1:n.81+1986G>A
ENST00000678297.1:c.*223G>A	ENSP00000503472.1:n.*223G>A
ENST00000678861.1:c.322G>A	ENSP00000502932.1:n.322G>A
ENST00000299697.11:c.*223G>A	ENSP00000299697.8:n.*223G>A
ENST00000451102.6:c.*223G>A	ENSP00000414334.3:n.*223G>A
ENST00000525974.5:c.*223G>A	ENSP00000434594.1:n.*223G>A
ENST00000527284.5:c.*223G>A	ENSP00000435312.1:n.*223G>A
ENST00000527800.5:c.*223G>A	ENSP00000433770.1:n.*223G>A
ENST00000544898.5:c.*223G>A	ENSP00000440898.2:n.*223G>A
ENST00000545043.6:c.*223G>A	ENSP00000438143.2:n.*223G>A
ENST00000561527.5:n.258+1986G>A
ENST00000561728.1:c.148+1986G>A
ENST00000561905.2:c.53+1986G>A
ENST00000562552.5:n.837G>A
ENST00000563099.5:n.548G>A
ENST00000564917.5:c.*223G>A	ENSP00000455187.1:n.*223G>A
ENST00000567357.5:c.*879G>A	ENSP00000457959.1:n.*879G>A
ENST00000569718.5:c.746G>A
ENST00000620035.4:c.*223G>A	ENSP00000483833.1:n.*223G>A
NM_001172643.1:c.*223G>A	NP_001166114.1:n.*223G>A
NM_001172644.1:c.*223G>A	NP_001166115.1:n.*223G>A
NM_001172645.1:c.*223G>A	NP_001166116.1:n.*223G>A
NM_001271934.1:c.*223G>A	NP_001258863.1:n.*223G>A
NM_001271935.1:c.*318G>A	NP_001258864.1:n.*318G>A
NM_001272050.1:c.*223G>A	NP_001258979.1:n.*223G>A
NM_004614.4:c.*223G>A	NP_004605.4:n.*223G>A
NR_073520.1:n.2300G>A
NM_001172644.2:c.*223G>A	NP_001166115.1:n.*223G>A
NM_001271934.2:c.*223G>A	NP_001258863.1:n.*223G>A
NM_001272050.2:c.*223G>A	NP_001258979.1:n.*223G>A
NM_004614.5:c.*223G>A MANE Select	NP_004605.4:n.*223G>A
NR_073520.2:n.2010G>A
NM_001172645.2:c.*223G>A	NP_001166116.1:n.*223G>A