Canonical Allele Identifier: CA282173412

Gene: TK2

Linked Data

• dbSNP Id: rs755982975
• gnomAD v2: 16-66547263-CCAAA-C
• gnomAD v3: 16-66513360-CCAAA-C
• gnomAD v4: 16-66513360-CCAAA-C
• MyVariant Identifiers: chr16:g.66547264_66547267del (hg19) ; chr16:g.66513361_66513364del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513365_66513368del , CM000678.2:g.66513365_66513368del	GRCh38
NC_000016.9:g.66547268_66547271del , CM000678.1:g.66547268_66547271del	GRCh37
NC_000016.8:g.65104769_65104772del	NCBI36
NG_016862.1:g.42049_42052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.531+367_531+370del	ENSP00000299697.9:n.531+367_531+370del
ENST00000417693.8:c.645+367_645+370del	ENSP00000407469.5:n.645+367_645+370del
ENST00000451102.7:c.606+367_606+370del	ENSP00000414334.4:n.606+367_606+370del
ENST00000527284.6:c.563-1298_563-1295del
ENST00000527800.6:c.408+367_408+370del	ENSP00000433770.1:n.408+367_408+370del
ENST00000544898.6:c.699+367_699+370del MANE Select	ENSP00000440898.2:n.699+367_699+370del
ENST00000567357.6:c.*557+367_*557+370del	ENSP00000457959.2:n.*557+367_*557+370del
ENST00000569718.6:c.437+367_437+370del	ENSP00000464313.2:n.437+367_437+370del
ENST00000620035.5:c.455+367_455+370del	ENSP00000483833.2:n.455+367_455+370del
ENST00000677296.1:n.82-240_82-237del
ENST00000677420.1:c.408+367_408+370del	ENSP00000504648.1:n.408+367_408+370del
ENST00000677555.1:c.408+367_408+370del	ENSP00000503331.1:n.408+367_408+370del
ENST00000677715.1:c.408+367_408+370del	ENSP00000502950.1:n.408+367_408+370del
ENST00000677753.1:n.81+367_81+370del
ENST00000678015.1:c.408+367_408+370del	ENSP00000502959.1:n.408+367_408+370del
ENST00000678190.1:c.82-13_82-10del	ENSP00000503824.1:n.82-13_82-10del
ENST00000678282.1:n.81+367_81+370del
ENST00000678297.1:c.408+367_408+370del	ENSP00000503472.1:n.408+367_408+370del
ENST00000299697.11:c.699+367_699+370del	ENSP00000299697.8:n.699+367_699+370del
ENST00000417693.7:c.771+367_771+370del	ENSP00000407469.4:n.771+367_771+370del
ENST00000451102.6:c.825+367_825+370del	ENSP00000414334.3:n.825+367_825+370del
ENST00000525974.5:c.408+367_408+370del	ENSP00000434594.1:n.408+367_408+370del
ENST00000527284.5:c.606+367_606+370del	ENSP00000435312.1:n.606+367_606+370del
ENST00000527800.5:c.408+367_408+370del	ENSP00000433770.1:n.408+367_408+370del
ENST00000544898.5:c.699+367_699+370del	ENSP00000440898.2:n.699+367_699+370del
ENST00000545043.6:c.624+367_624+370del	ENSP00000438143.2:n.624+367_624+370del
ENST00000561527.5:n.258+367_258+370del
ENST00000561728.1:c.148+367_148+370del
ENST00000561905.2:c.53+367_53+370del
ENST00000562552.5:n.515+367_515+370del
ENST00000563099.5:n.226+367_226+370del
ENST00000563369.6:c.408+367_408+370del	ENSP00000463560.1:n.408+367_408+370del
ENST00000564792.1:n.354+367_354+370del
ENST00000564917.5:c.750+367_750+370del	ENSP00000455187.1:n.750+367_750+370del
ENST00000567357.5:c.*557+367_*557+370del	ENSP00000457959.1:n.*557+367_*557+370del
ENST00000569718.5:c.424+367_424+370del
ENST00000620035.4:c.645+367_645+370del	ENSP00000483833.1:n.645+367_645+370del
NM_001172643.1:c.606+367_606+370del	NP_001166114.1:n.606+367_606+370del
NM_001172644.1:c.624+367_624+370del	NP_001166115.1:n.624+367_624+370del
NM_001172645.1:c.645+367_645+370del	NP_001166116.1:n.645+367_645+370del
NM_001271934.1:c.552+367_552+370del	NP_001258863.1:n.552+367_552+370del
NM_001271935.1:c.437+367_437+370del	NP_001258864.1:n.437+367_437+370del
NM_001272050.1:c.408+367_408+370del	NP_001258979.1:n.408+367_408+370del
NM_004614.4:c.699+367_699+370del	NP_004605.4:n.699+367_699+370del
NR_073520.1:n.1978+367_1978+370del
NM_001172644.2:c.624+367_624+370del	NP_001166115.1:n.624+367_624+370del
NM_001271934.2:c.552+367_552+370del	NP_001258863.1:n.552+367_552+370del
NM_001272050.2:c.408+367_408+370del	NP_001258979.1:n.408+367_408+370del
NM_004614.5:c.699+367_699+370del MANE Select	NP_004605.4:n.699+367_699+370del
NR_073520.2:n.1688+367_1688+370del
NM_001172645.2:c.645+367_645+370del	NP_001166116.1:n.645+367_645+370del