Canonical Allele Identifier: CA396187101

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547657A>C (hg19) ; chr16:g.66513754A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513754A>C , CM000678.2:g.66513754A>C	GRCh38
NC_000016.9:g.66547657A>C , CM000678.1:g.66547657A>C	GRCh37
NC_000016.8:g.65105158A>C	NCBI36
NG_016862.1:g.41659T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.508T>G	ENSP00000299697.9:p.Phe170Val
ENST00000417693.8:c.622T>G	ENSP00000407469.5:p.Phe208Val
ENST00000451102.7:c.583T>G	ENSP00000414334.4:p.Phe195Val
ENST00000527284.6:c.563-1688T>G
ENST00000527800.6:c.385T>G	ENSP00000433770.1:p.Phe129Val
ENST00000544898.6:c.676T>G MANE Select	ENSP00000440898.2:p.Phe226Val
ENST00000567357.6:c.*534T>G	ENSP00000457959.2:n.*534T>G
ENST00000569718.6:c.414T>G	ENSP00000464313.2:p.Phe138Leu
ENST00000620035.5:c.432T>G	ENSP00000483833.2:p.Phe144Leu
ENST00000676538.1:c.259T>G
ENST00000676904.1:c.147T>G
ENST00000677296.1:n.58T>G
ENST00000677379.1:c.317T>G	ENSP00000503672.1:n.317T>G
ENST00000677420.1:c.385T>G	ENSP00000504648.1:p.Phe129Val
ENST00000677555.1:c.385T>G	ENSP00000503331.1:p.Phe129Val
ENST00000677715.1:c.385T>G	ENSP00000502950.1:p.Phe129Val
ENST00000677753.1:n.58T>G
ENST00000677961.1:n.88T>G
ENST00000678015.1:c.385T>G	ENSP00000502959.1:p.Phe129Val
ENST00000678190.1:c.58T>G	ENSP00000503824.1:p.Phe20Val
ENST00000678282.1:n.58T>G
ENST00000678297.1:c.385T>G	ENSP00000503472.1:p.Phe129Val
ENST00000299697.11:c.676T>G	ENSP00000299697.8:p.Phe226Val
ENST00000417693.7:c.748T>G	ENSP00000407469.4:p.Phe250Val
ENST00000451102.6:c.802T>G	ENSP00000414334.3:p.Phe268Val
ENST00000525974.5:c.385T>G	ENSP00000434594.1:p.Phe129Val
ENST00000527284.5:c.583T>G	ENSP00000435312.1:p.Phe195Val
ENST00000527800.5:c.385T>G	ENSP00000433770.1:p.Phe129Val
ENST00000544898.5:c.676T>G	ENSP00000440898.2:p.Phe226Val
ENST00000545043.6:c.601T>G	ENSP00000438143.2:p.Phe201Val
ENST00000561527.5:n.235T>G
ENST00000561728.1:c.125T>G
ENST00000561905.2:c.30T>G
ENST00000562552.5:n.492T>G
ENST00000563099.5:n.203T>G
ENST00000563369.6:c.385T>G	ENSP00000463560.1:p.Phe129Val
ENST00000563478.5:c.385T>G	ENSP00000462341.1:p.Phe129Val
ENST00000564792.1:n.331T>G
ENST00000564917.5:c.727T>G	ENSP00000455187.1:p.Phe243Val
ENST00000567357.5:c.*534T>G	ENSP00000457959.1:n.*534T>G
ENST00000569718.5:c.401T>G
ENST00000620035.4:c.622T>G	ENSP00000483833.1:p.Phe208Val
NM_001172643.1:c.583T>G	NP_001166114.1:p.Phe195Val
NM_001172644.1:c.601T>G	NP_001166115.1:p.Phe201Val
NM_001172645.1:c.622T>G	NP_001166116.1:p.Phe208Val
NM_001271934.1:c.529T>G	NP_001258863.1:p.Phe177Val
NM_001271935.1:c.414T>G	NP_001258864.1:p.Phe138Leu
NM_001272050.1:c.385T>G	NP_001258979.1:p.Phe129Val
NM_004614.4:c.676T>G	NP_004605.4:p.Phe226Val
NR_073520.1:n.1955T>G
NM_001172644.2:c.601T>G	NP_001166115.1:p.Phe201Val
NM_001271934.2:c.529T>G	NP_001258863.1:p.Phe177Val
NM_001272050.2:c.385T>G	NP_001258979.1:p.Phe129Val
NM_004614.5:c.676T>G MANE Select	NP_004605.4:p.Phe226Val
NR_073520.2:n.1665T>G
NM_001172645.2:c.622T>G	NP_001166116.1:p.Phe208Val