Canonical Allele Identifier: CA2633652659

Gene: TK2

Linked Data

• gnomAD v4: 16-66531357-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531360del , CM000678.2:g.66531360del	GRCh38
NC_000016.9:g.66565263del , CM000678.1:g.66565263del	GRCh37
NC_000016.8:g.65122764del	NCBI36
NG_016862.1:g.24055del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.207+22del	ENSP00000299697.9:n.207+22del
ENST00000417693.8:c.321+22del	ENSP00000407469.5:n.321+22del
ENST00000451102.7:c.282+22del	ENSP00000414334.4:n.282+22del
ENST00000527284.6:c.319+22del
ENST00000527800.6:c.84+22del	ENSP00000433770.1:n.84+22del
ENST00000544898.6:c.375+22del MANE Select	ENSP00000440898.2:n.375+22del
ENST00000567357.6:c.*233+22del	ENSP00000457959.2:n.*233+22del
ENST00000569718.6:c.282+22del	ENSP00000464313.2:n.282+22del
ENST00000620035.5:c.300+22del	ENSP00000483833.2:n.300+22del
ENST00000676538.1:c.33-13481del
ENST00000677379.1:c.90+22del	ENSP00000503672.1:n.90+22del
ENST00000677420.1:c.84+22del	ENSP00000504648.1:n.84+22del
ENST00000677555.1:c.84+22del	ENSP00000503331.1:n.84+22del
ENST00000677715.1:c.84+22del	ENSP00000502950.1:n.84+22del
ENST00000677739.1:c.55-2291del	ENSP00000504644.1:n.55-2291del
ENST00000678015.1:c.84+22del	ENSP00000502959.1:n.84+22del
ENST00000678297.1:c.84+22del	ENSP00000503472.1:n.84+22del
ENST00000678314.1:c.84+22del	ENSP00000504438.1:n.84+22del
ENST00000678746.1:c.265+22del	ENSP00000503227.1:n.265+22del
ENST00000299697.11:c.375+22del	ENSP00000299697.8:n.375+22del
ENST00000417693.7:c.447+22del	ENSP00000407469.4:n.447+22del
ENST00000451102.6:c.501+22del	ENSP00000414334.3:n.501+22del
ENST00000525974.5:c.84+22del	ENSP00000434594.1:n.84+22del
ENST00000527284.5:c.282+22del	ENSP00000435312.1:n.282+22del
ENST00000527800.5:c.84+22del	ENSP00000433770.1:n.84+22del
ENST00000544898.5:c.375+22del	ENSP00000440898.2:n.375+22del
ENST00000545043.6:c.300+22del	ENSP00000438143.2:n.300+22del
ENST00000562484.2:c.84+22del	ENSP00000463326.1:n.84+22del
ENST00000563369.6:c.84+22del	ENSP00000463560.1:n.84+22del
ENST00000563478.5:c.84+22del	ENSP00000462341.1:n.84+22del
ENST00000564917.5:c.375+22del	ENSP00000455187.1:n.375+22del
ENST00000567357.5:c.*233+22del	ENSP00000457959.1:n.*233+22del
ENST00000569718.5:c.269+22del
ENST00000620035.4:c.321+22del	ENSP00000483833.1:n.321+22del
NM_001172643.1:c.282+22del	NP_001166114.1:n.282+22del
NM_001172644.1:c.300+22del	NP_001166115.1:n.300+22del
NM_001172645.1:c.321+22del	NP_001166116.1:n.321+22del
NM_001271934.1:c.228+22del	NP_001258863.1:n.228+22del
NM_001271935.1:c.282+22del	NP_001258864.1:n.282+22del
NM_001272050.1:c.84+22del	NP_001258979.1:n.84+22del
NM_004614.4:c.375+22del	NP_004605.4:n.375+22del
NR_073520.1:n.1654+22del
NM_001172644.2:c.300+22del	NP_001166115.1:n.300+22del
NM_001271934.2:c.228+22del	NP_001258863.1:n.228+22del
NM_001272050.2:c.84+22del	NP_001258979.1:n.84+22del
NM_004614.5:c.375+22del MANE Select	NP_004605.4:n.375+22del
NR_073520.2:n.1364+22del
NM_001172645.2:c.321+22del	NP_001166116.1:n.321+22del