Canonical Allele Identifier: CA2633622740
Gene: TK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66513728_66513743del , CM000678.2:g.66513728_66513743del GRCh38
NC_000016.9:g.66547631_66547646del , CM000678.1:g.66547631_66547646del GRCh37
NC_000016.8:g.65105132_65105147del NCBI36
NG_016862.1:g.41672_41687del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.521_531+5del
ENST00000417693.8:c.635_645+5del
ENST00000451102.7:c.596_606+5del
ENST00000527284.6:c.563-1675_563-1660del
ENST00000527800.6:c.398_408+5del
ENST00000544898.6:c.689_699+5del
ENST00000567357.6:c.*547_*557+5del
ENST00000569718.6:c.427_437+5del
ENST00000620035.5:c.445_455+5del
ENST00000677296.1:n.71_81+5del
ENST00000677420.1:c.398_408+5del
ENST00000677555.1:c.398_408+5del
ENST00000677715.1:c.398_408+5del
ENST00000677753.1:n.71_81+5del
ENST00000678015.1:c.398_408+5del
ENST00000678190.1:c.71_81+5del
ENST00000678282.1:n.71_81+5del
ENST00000678297.1:c.398_408+5del
ENST00000299697.11:c.689_699+5del
ENST00000417693.7:c.761_771+5del
ENST00000451102.6:c.815_825+5del
ENST00000525974.5:c.398_408+5del
ENST00000527284.5:c.596_606+5del
ENST00000527800.5:c.398_408+5del
ENST00000544898.5:c.689_699+5del
ENST00000545043.6:c.614_624+5del
ENST00000561527.5:n.248_258+5del
ENST00000561728.1:c.138_148+5del
ENST00000561905.2:c.43_53+5del
ENST00000562552.5:n.505_515+5del
ENST00000563099.5:n.216_226+5del
ENST00000563369.6:c.398_408+5del
ENST00000564792.1:n.344_354+5del
ENST00000564917.5:c.740_750+5del
ENST00000567357.5:c.*547_*557+5del
ENST00000569718.5:c.414_424+5del
ENST00000620035.4:c.635_645+5del
NM_001172643.1:c.596_606+5del
NM_001172644.1:c.614_624+5del
NM_001172645.1:c.635_645+5del
NM_001271934.1:c.542_552+5del
NM_001271935.1:c.427_437+5del
NM_001272050.1:c.398_408+5del
NM_004614.4:c.689_699+5del
NR_073520.1:n.1968_1978+5del
NM_001172644.2:c.614_624+5del
NM_001271934.2:c.542_552+5del
NM_001272050.2:c.398_408+5del
NM_004614.5:c.689_699+5del
NR_073520.2:n.1678_1688+5del
NM_001172645.2:c.635_645+5del