Canonical Allele Identifier: CA2228908752

Gene: TK2

Linked Data

• dbSNP Id: rs1964507815

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513365_66513367del , CM000678.2:g.66513365_66513367del	GRCh38
NC_000016.9:g.66547268_66547270del , CM000678.1:g.66547268_66547270del	GRCh37
NC_000016.8:g.65104769_65104771del	NCBI36
NG_016862.1:g.42048_42050del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.531+366_531+368del	ENSP00000299697.9:n.531+366_531+368del
ENST00000417693.8:c.645+366_645+368del	ENSP00000407469.5:n.645+366_645+368del
ENST00000451102.7:c.606+366_606+368del	ENSP00000414334.4:n.606+366_606+368del
ENST00000527284.6:c.563-1299_563-1297del
ENST00000527800.6:c.408+366_408+368del	ENSP00000433770.1:n.408+366_408+368del
ENST00000544898.6:c.699+366_699+368del MANE Select	ENSP00000440898.2:n.699+366_699+368del
ENST00000567357.6:c.*557+366_*557+368del	ENSP00000457959.2:n.*557+366_*557+368del
ENST00000569718.6:c.437+366_437+368del	ENSP00000464313.2:n.437+366_437+368del
ENST00000620035.5:c.455+366_455+368del	ENSP00000483833.2:n.455+366_455+368del
ENST00000677296.1:n.82-241_82-239del
ENST00000677420.1:c.408+366_408+368del	ENSP00000504648.1:n.408+366_408+368del
ENST00000677555.1:c.408+366_408+368del	ENSP00000503331.1:n.408+366_408+368del
ENST00000677715.1:c.408+366_408+368del	ENSP00000502950.1:n.408+366_408+368del
ENST00000677753.1:n.81+366_81+368del
ENST00000678015.1:c.408+366_408+368del	ENSP00000502959.1:n.408+366_408+368del
ENST00000678190.1:c.82-14_82-12del	ENSP00000503824.1:n.82-14_82-12del
ENST00000678282.1:n.81+366_81+368del
ENST00000678297.1:c.408+366_408+368del	ENSP00000503472.1:n.408+366_408+368del
ENST00000299697.11:c.699+366_699+368del	ENSP00000299697.8:n.699+366_699+368del
ENST00000417693.7:c.771+366_771+368del	ENSP00000407469.4:n.771+366_771+368del
ENST00000451102.6:c.825+366_825+368del	ENSP00000414334.3:n.825+366_825+368del
ENST00000525974.5:c.408+366_408+368del	ENSP00000434594.1:n.408+366_408+368del
ENST00000527284.5:c.606+366_606+368del	ENSP00000435312.1:n.606+366_606+368del
ENST00000527800.5:c.408+366_408+368del	ENSP00000433770.1:n.408+366_408+368del
ENST00000544898.5:c.699+366_699+368del	ENSP00000440898.2:n.699+366_699+368del
ENST00000545043.6:c.624+366_624+368del	ENSP00000438143.2:n.624+366_624+368del
ENST00000561527.5:n.258+366_258+368del
ENST00000561728.1:c.148+366_148+368del
ENST00000561905.2:c.53+366_53+368del
ENST00000562552.5:n.515+366_515+368del
ENST00000563099.5:n.226+366_226+368del
ENST00000563369.6:c.408+366_408+368del	ENSP00000463560.1:n.408+366_408+368del
ENST00000564792.1:n.354+366_354+368del
ENST00000564917.5:c.750+366_750+368del	ENSP00000455187.1:n.750+366_750+368del
ENST00000567357.5:c.*557+366_*557+368del	ENSP00000457959.1:n.*557+366_*557+368del
ENST00000569718.5:c.424+366_424+368del
ENST00000620035.4:c.645+366_645+368del	ENSP00000483833.1:n.645+366_645+368del
NM_001172643.1:c.606+366_606+368del	NP_001166114.1:n.606+366_606+368del
NM_001172644.1:c.624+366_624+368del	NP_001166115.1:n.624+366_624+368del
NM_001172645.1:c.645+366_645+368del	NP_001166116.1:n.645+366_645+368del
NM_001271934.1:c.552+366_552+368del	NP_001258863.1:n.552+366_552+368del
NM_001271935.1:c.437+366_437+368del	NP_001258864.1:n.437+366_437+368del
NM_001272050.1:c.408+366_408+368del	NP_001258979.1:n.408+366_408+368del
NM_004614.4:c.699+366_699+368del	NP_004605.4:n.699+366_699+368del
NR_073520.1:n.1978+366_1978+368del
NM_001172644.2:c.624+366_624+368del	NP_001166115.1:n.624+366_624+368del
NM_001271934.2:c.552+366_552+368del	NP_001258863.1:n.552+366_552+368del
NM_001272050.2:c.408+366_408+368del	NP_001258979.1:n.408+366_408+368del
NM_004614.5:c.699+366_699+368del MANE Select	NP_004605.4:n.699+366_699+368del
NR_073520.2:n.1688+366_1688+368del
NM_001172645.2:c.645+366_645+368del	NP_001166116.1:n.645+366_645+368del