Canonical Allele Identifier: CA2633622651

Gene: TK2

Linked Data

• gnomAD v4: 16-66513580-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513588_66513589dup , CM000678.2:g.66513588_66513589dup	GRCh38
NC_000016.9:g.66547491_66547492dup , CM000678.1:g.66547491_66547492dup	GRCh37
NC_000016.8:g.65104992_65104993dup	NCBI36
NG_016862.1:g.41831_41832dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.531+149_531+150dup	ENSP00000299697.9:n.531+149_531+150dup
ENST00000417693.8:c.645+149_645+150dup	ENSP00000407469.5:n.645+149_645+150dup
ENST00000451102.7:c.606+149_606+150dup	ENSP00000414334.4:n.606+149_606+150dup
ENST00000527284.6:c.563-1516_563-1515dup
ENST00000527800.6:c.408+149_408+150dup	ENSP00000433770.1:n.408+149_408+150dup
ENST00000544898.6:c.699+149_699+150dup MANE Select	ENSP00000440898.2:n.699+149_699+150dup
ENST00000567357.6:c.*557+149_*557+150dup	ENSP00000457959.2:n.*557+149_*557+150dup
ENST00000569718.6:c.437+149_437+150dup	ENSP00000464313.2:n.437+149_437+150dup
ENST00000620035.5:c.455+149_455+150dup	ENSP00000483833.2:n.455+149_455+150dup
ENST00000677296.1:n.81+149_81+150dup
ENST00000677420.1:c.408+149_408+150dup	ENSP00000504648.1:n.408+149_408+150dup
ENST00000677555.1:c.408+149_408+150dup	ENSP00000503331.1:n.408+149_408+150dup
ENST00000677715.1:c.408+149_408+150dup	ENSP00000502950.1:n.408+149_408+150dup
ENST00000677753.1:n.81+149_81+150dup
ENST00000678015.1:c.408+149_408+150dup	ENSP00000502959.1:n.408+149_408+150dup
ENST00000678190.1:c.81+149_81+150dup	ENSP00000503824.1:n.81+149_81+150dup
ENST00000678282.1:n.81+149_81+150dup
ENST00000678297.1:c.408+149_408+150dup	ENSP00000503472.1:n.408+149_408+150dup
ENST00000299697.11:c.699+149_699+150dup	ENSP00000299697.8:n.699+149_699+150dup
ENST00000417693.7:c.771+149_771+150dup	ENSP00000407469.4:n.771+149_771+150dup
ENST00000451102.6:c.825+149_825+150dup	ENSP00000414334.3:n.825+149_825+150dup
ENST00000525974.5:c.408+149_408+150dup	ENSP00000434594.1:n.408+149_408+150dup
ENST00000527284.5:c.606+149_606+150dup	ENSP00000435312.1:n.606+149_606+150dup
ENST00000527800.5:c.408+149_408+150dup	ENSP00000433770.1:n.408+149_408+150dup
ENST00000544898.5:c.699+149_699+150dup	ENSP00000440898.2:n.699+149_699+150dup
ENST00000545043.6:c.624+149_624+150dup	ENSP00000438143.2:n.624+149_624+150dup
ENST00000561527.5:n.258+149_258+150dup
ENST00000561728.1:c.148+149_148+150dup
ENST00000561905.2:c.53+149_53+150dup
ENST00000562552.5:n.515+149_515+150dup
ENST00000563099.5:n.226+149_226+150dup
ENST00000563369.6:c.408+149_408+150dup	ENSP00000463560.1:n.408+149_408+150dup
ENST00000564792.1:n.354+149_354+150dup
ENST00000564917.5:c.750+149_750+150dup	ENSP00000455187.1:n.750+149_750+150dup
ENST00000567357.5:c.*557+149_*557+150dup	ENSP00000457959.1:n.*557+149_*557+150dup
ENST00000569718.5:c.424+149_424+150dup
ENST00000620035.4:c.645+149_645+150dup	ENSP00000483833.1:n.645+149_645+150dup
NM_001172643.1:c.606+149_606+150dup	NP_001166114.1:n.606+149_606+150dup
NM_001172644.1:c.624+149_624+150dup	NP_001166115.1:n.624+149_624+150dup
NM_001172645.1:c.645+149_645+150dup	NP_001166116.1:n.645+149_645+150dup
NM_001271934.1:c.552+149_552+150dup	NP_001258863.1:n.552+149_552+150dup
NM_001271935.1:c.437+149_437+150dup	NP_001258864.1:n.437+149_437+150dup
NM_001272050.1:c.408+149_408+150dup	NP_001258979.1:n.408+149_408+150dup
NM_004614.4:c.699+149_699+150dup	NP_004605.4:n.699+149_699+150dup
NR_073520.1:n.1978+149_1978+150dup
NM_001172644.2:c.624+149_624+150dup	NP_001166115.1:n.624+149_624+150dup
NM_001271934.2:c.552+149_552+150dup	NP_001258863.1:n.552+149_552+150dup
NM_001272050.2:c.408+149_408+150dup	NP_001258979.1:n.408+149_408+150dup
NM_004614.5:c.699+149_699+150dup MANE Select	NP_004605.4:n.699+149_699+150dup
NR_073520.2:n.1688+149_1688+150dup
NM_001172645.2:c.645+149_645+150dup	NP_001166116.1:n.645+149_645+150dup