Canonical Allele Identifier: CA2633622833

Gene: TK2

Linked Data

• gnomAD v4: 16-66513980-CACACT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513981_66513985del , CM000678.2:g.66513981_66513985del	GRCh38
NC_000016.9:g.66547884_66547888del , CM000678.1:g.66547884_66547888del	GRCh37
NC_000016.8:g.65105385_65105389del	NCBI36
NG_016862.1:g.41428_41432del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.451-174_451-170del	ENSP00000299697.9:n.451-174_451-170del
ENST00000417693.8:c.565-174_565-170del	ENSP00000407469.5:n.565-174_565-170del
ENST00000451102.7:c.526-174_526-170del	ENSP00000414334.4:n.526-174_526-170del
ENST00000527284.6:c.563-1919_563-1915del
ENST00000527800.6:c.328-174_328-170del	ENSP00000433770.1:n.328-174_328-170del
ENST00000544898.6:c.619-174_619-170del MANE Select	ENSP00000440898.2:n.619-174_619-170del
ENST00000567357.6:c.*477-174_*477-170del	ENSP00000457959.2:n.*477-174_*477-170del
ENST00000569718.6:c.357-174_357-170del	ENSP00000464313.2:n.357-174_357-170del
ENST00000620035.5:c.375-174_375-170del	ENSP00000483833.2:n.375-174_375-170del
ENST00000676538.1:c.202-174_202-170del
ENST00000676904.1:c.90-174_90-170del
ENST00000677379.1:c.260-174_260-170del	ENSP00000503672.1:n.260-174_260-170del
ENST00000677420.1:c.328-174_328-170del	ENSP00000504648.1:n.328-174_328-170del
ENST00000677555.1:c.328-174_328-170del	ENSP00000503331.1:n.328-174_328-170del
ENST00000677715.1:c.328-174_328-170del	ENSP00000502950.1:n.328-174_328-170del
ENST00000678015.1:c.328-174_328-170del	ENSP00000502959.1:n.328-174_328-170del
ENST00000678297.1:c.328-174_328-170del	ENSP00000503472.1:n.328-174_328-170del
ENST00000299697.11:c.619-174_619-170del	ENSP00000299697.8:n.619-174_619-170del
ENST00000417693.7:c.691-174_691-170del	ENSP00000407469.4:n.691-174_691-170del
ENST00000451102.6:c.745-174_745-170del	ENSP00000414334.3:n.745-174_745-170del
ENST00000525974.5:c.328-174_328-170del	ENSP00000434594.1:n.328-174_328-170del
ENST00000527284.5:c.526-174_526-170del	ENSP00000435312.1:n.526-174_526-170del
ENST00000527800.5:c.328-174_328-170del	ENSP00000433770.1:n.328-174_328-170del
ENST00000544898.5:c.619-174_619-170del	ENSP00000440898.2:n.619-174_619-170del
ENST00000545043.6:c.544-174_544-170del	ENSP00000438143.2:n.544-174_544-170del
ENST00000561527.5:n.178-174_178-170del
ENST00000561728.1:c.68-174_68-170del
ENST00000562552.5:n.435-174_435-170del
ENST00000563099.5:n.146-174_146-170del
ENST00000563369.6:c.328-174_328-170del	ENSP00000463560.1:n.328-174_328-170del
ENST00000563478.5:c.328-174_328-170del	ENSP00000462341.1:n.328-174_328-170del
ENST00000564792.1:n.274-174_274-170del
ENST00000564917.5:c.619-123_619-119del	ENSP00000455187.1:n.619-123_619-119del
ENST00000567357.5:c.*477-174_*477-170del	ENSP00000457959.1:n.*477-174_*477-170del
ENST00000569718.5:c.344-174_344-170del
ENST00000620035.4:c.565-174_565-170del	ENSP00000483833.1:n.565-174_565-170del
NM_001172643.1:c.526-174_526-170del	NP_001166114.1:n.526-174_526-170del
NM_001172644.1:c.544-174_544-170del	NP_001166115.1:n.544-174_544-170del
NM_001172645.1:c.565-174_565-170del	NP_001166116.1:n.565-174_565-170del
NM_001271934.1:c.472-174_472-170del	NP_001258863.1:n.472-174_472-170del
NM_001271935.1:c.357-174_357-170del	NP_001258864.1:n.357-174_357-170del
NM_001272050.1:c.328-174_328-170del	NP_001258979.1:n.328-174_328-170del
NM_004614.4:c.619-174_619-170del	NP_004605.4:n.619-174_619-170del
NR_073520.1:n.1898-174_1898-170del
NM_001172644.2:c.544-174_544-170del	NP_001166115.1:n.544-174_544-170del
NM_001271934.2:c.472-174_472-170del	NP_001258863.1:n.472-174_472-170del
NM_001272050.2:c.328-174_328-170del	NP_001258979.1:n.328-174_328-170del
NM_004614.5:c.619-174_619-170del MANE Select	NP_004605.4:n.619-174_619-170del
NR_073520.2:n.1608-174_1608-170del
NM_001172645.2:c.565-174_565-170del	NP_001166116.1:n.565-174_565-170del