Canonical Allele Identifier: CA495902935

Gene: TK2

Linked Data

• dbSNP Id: rs2144339612
• MyVariant Identifiers: chr16:g.66547643G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513740G>C , CM000678.2:g.66513740G>C	GRCh38
NC_000016.9:g.66547643G>C , CM000678.1:g.66547643G>C	GRCh37
NC_000016.8:g.65105144G>C	NCBI36
NG_016862.1:g.41673C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.522C>G	ENSP00000299697.9:p.Ala174=
ENST00000417693.8:c.636C>G	ENSP00000407469.5:p.Ala212=
ENST00000451102.7:c.597C>G	ENSP00000414334.4:p.Ala199=
ENST00000527284.6:c.563-1674C>G
ENST00000527800.6:c.399C>G	ENSP00000433770.1:p.Ala133=
ENST00000544898.6:c.690C>G MANE Select	ENSP00000440898.2:p.Ala230=
ENST00000567357.6:c.*548C>G	ENSP00000457959.2:n.*548C>G
ENST00000569718.6:c.428C>G	ENSP00000464313.2:p.Pro143Arg
ENST00000620035.5:c.446C>G	ENSP00000483833.2:p.Pro149Arg
ENST00000676538.1:c.273C>G
ENST00000676904.1:c.161C>G
ENST00000677296.1:n.72C>G
ENST00000677379.1:c.331C>G	ENSP00000503672.1:n.331C>G
ENST00000677420.1:c.399C>G	ENSP00000504648.1:p.Ala133=
ENST00000677555.1:c.399C>G	ENSP00000503331.1:p.Ala133=
ENST00000677715.1:c.399C>G	ENSP00000502950.1:p.Ala133=
ENST00000677753.1:n.72C>G
ENST00000677961.1:n.102C>G
ENST00000678015.1:c.399C>G	ENSP00000502959.1:p.Ala133=
ENST00000678190.1:c.72C>G	ENSP00000503824.1:p.Ala24=
ENST00000678282.1:n.72C>G
ENST00000678297.1:c.399C>G	ENSP00000503472.1:p.Ala133=
ENST00000299697.11:c.690C>G	ENSP00000299697.8:p.Ala230=
ENST00000417693.7:c.762C>G	ENSP00000407469.4:p.Ala254=
ENST00000451102.6:c.816C>G	ENSP00000414334.3:p.Ala272=
ENST00000525974.5:c.399C>G	ENSP00000434594.1:p.Ala133=
ENST00000527284.5:c.597C>G	ENSP00000435312.1:p.Ala199=
ENST00000527800.5:c.399C>G	ENSP00000433770.1:p.Ala133=
ENST00000544898.5:c.690C>G	ENSP00000440898.2:p.Ala230=
ENST00000545043.6:c.615C>G	ENSP00000438143.2:p.Ala205=
ENST00000561527.5:n.249C>G
ENST00000561728.1:c.139C>G
ENST00000561905.2:c.44C>G
ENST00000562552.5:n.506C>G
ENST00000563099.5:n.217C>G
ENST00000563369.6:c.399C>G	ENSP00000463560.1:p.Ala133=
ENST00000564792.1:n.345C>G
ENST00000564917.5:c.741C>G	ENSP00000455187.1:p.Ala247=
ENST00000567357.5:c.*548C>G	ENSP00000457959.1:n.*548C>G
ENST00000569718.5:c.415C>G
ENST00000620035.4:c.636C>G	ENSP00000483833.1:p.Ala212=
NM_001172643.1:c.597C>G	NP_001166114.1:p.Ala199=
NM_001172644.1:c.615C>G	NP_001166115.1:p.Ala205=
NM_001172645.1:c.636C>G	NP_001166116.1:p.Ala212=
NM_001271934.1:c.543C>G	NP_001258863.1:p.Ala181=
NM_001271935.1:c.428C>G	NP_001258864.1:p.Pro143Arg
NM_001272050.1:c.399C>G	NP_001258979.1:p.Ala133=
NM_004614.4:c.690C>G	NP_004605.4:p.Ala230=
NR_073520.1:n.1969C>G
NM_001172644.2:c.615C>G	NP_001166115.1:p.Ala205=
NM_001271934.2:c.543C>G	NP_001258863.1:p.Ala181=
NM_001272050.2:c.399C>G	NP_001258979.1:p.Ala133=
NM_004614.5:c.690C>G MANE Select	NP_004605.4:p.Ala230=
NR_073520.2:n.1679C>G
NM_001172645.2:c.636C>G	NP_001166116.1:p.Ala212=