Canonical Allele Identifier: CA2732485862

Gene: TK2

Linked Data

• dbSNP Id: rs2144408490

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531161_66531194del , CM000678.2:g.66531161_66531194del	GRCh38
NC_000016.9:g.66565064_66565097del , CM000678.1:g.66565064_66565097del	GRCh37
NC_000016.8:g.65122565_65122598del	NCBI36
NG_016862.1:g.24219_24252del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.207+186_207+219del	ENSP00000299697.9:n.207+186_207+219del
ENST00000417693.8:c.321+186_321+219del	ENSP00000407469.5:n.321+186_321+219del
ENST00000451102.7:c.282+186_282+219del	ENSP00000414334.4:n.282+186_282+219del
ENST00000527284.6:c.319+186_319+219del
ENST00000527800.6:c.84+186_84+219del	ENSP00000433770.1:n.84+186_84+219del
ENST00000544898.6:c.375+186_375+219del MANE Select	ENSP00000440898.2:n.375+186_375+219del
ENST00000567357.6:c.*233+186_*233+219del	ENSP00000457959.2:n.*233+186_*233+219del
ENST00000569718.6:c.282+186_282+219del	ENSP00000464313.2:n.282+186_282+219del
ENST00000620035.5:c.300+186_300+219del	ENSP00000483833.2:n.300+186_300+219del
ENST00000676538.1:c.33-13317_33-13284del
ENST00000677379.1:c.90+186_90+219del	ENSP00000503672.1:n.90+186_90+219del
ENST00000677420.1:c.84+186_84+219del	ENSP00000504648.1:n.84+186_84+219del
ENST00000677555.1:c.84+186_84+219del	ENSP00000503331.1:n.84+186_84+219del
ENST00000677715.1:c.84+186_84+219del	ENSP00000502950.1:n.84+186_84+219del
ENST00000677739.1:c.55-2127_55-2094del	ENSP00000504644.1:n.55-2127_55-2094del
ENST00000678015.1:c.84+186_84+219del	ENSP00000502959.1:n.84+186_84+219del
ENST00000678297.1:c.84+186_84+219del	ENSP00000503472.1:n.84+186_84+219del
ENST00000678314.1:c.84+186_84+219del	ENSP00000504438.1:n.84+186_84+219del
ENST00000678746.1:c.265+186_265+219del	ENSP00000503227.1:n.265+186_265+219del
ENST00000299697.11:c.375+186_375+219del	ENSP00000299697.8:n.375+186_375+219del
ENST00000417693.7:c.447+186_447+219del	ENSP00000407469.4:n.447+186_447+219del
ENST00000451102.6:c.501+186_501+219del	ENSP00000414334.3:n.501+186_501+219del
ENST00000525974.5:c.84+186_84+219del	ENSP00000434594.1:n.84+186_84+219del
ENST00000527284.5:c.282+186_282+219del	ENSP00000435312.1:n.282+186_282+219del
ENST00000527800.5:c.84+186_84+219del	ENSP00000433770.1:n.84+186_84+219del
ENST00000544898.5:c.375+186_375+219del	ENSP00000440898.2:n.375+186_375+219del
ENST00000545043.6:c.300+186_300+219del	ENSP00000438143.2:n.300+186_300+219del
ENST00000562484.2:c.84+186_84+219del	ENSP00000463326.1:n.84+186_84+219del
ENST00000563369.6:c.84+186_84+219del	ENSP00000463560.1:n.84+186_84+219del
ENST00000563478.5:c.84+186_84+219del	ENSP00000462341.1:n.84+186_84+219del
ENST00000564917.5:c.375+186_375+219del	ENSP00000455187.1:n.375+186_375+219del
ENST00000567357.5:c.*233+186_*233+219del	ENSP00000457959.1:n.*233+186_*233+219del
ENST00000569718.5:c.269+186_269+219del
ENST00000620035.4:c.321+186_321+219del	ENSP00000483833.1:n.321+186_321+219del
NM_001172643.1:c.282+186_282+219del	NP_001166114.1:n.282+186_282+219del
NM_001172644.1:c.300+186_300+219del	NP_001166115.1:n.300+186_300+219del
NM_001172645.1:c.321+186_321+219del	NP_001166116.1:n.321+186_321+219del
NM_001271934.1:c.228+186_228+219del	NP_001258863.1:n.228+186_228+219del
NM_001271935.1:c.282+186_282+219del	NP_001258864.1:n.282+186_282+219del
NM_001272050.1:c.84+186_84+219del	NP_001258979.1:n.84+186_84+219del
NM_004614.4:c.375+186_375+219del	NP_004605.4:n.375+186_375+219del
NR_073520.1:n.1654+186_1654+219del
NM_001172644.2:c.300+186_300+219del	NP_001166115.1:n.300+186_300+219del
NM_001271934.2:c.228+186_228+219del	NP_001258863.1:n.228+186_228+219del
NM_001272050.2:c.84+186_84+219del	NP_001258979.1:n.84+186_84+219del
NM_004614.5:c.375+186_375+219del MANE Select	NP_004605.4:n.375+186_375+219del
NR_073520.2:n.1364+186_1364+219del
NM_001172645.2:c.321+186_321+219del	NP_001166116.1:n.321+186_321+219del