Canonical Allele Identifier: CA396187030

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547638A>C (hg19) ; chr16:g.66513735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513735A>C , CM000678.2:g.66513735A>C	GRCh38
NC_000016.9:g.66547638A>C , CM000678.1:g.66547638A>C	GRCh37
NC_000016.8:g.65105139A>C	NCBI36
NG_016862.1:g.41678T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.527T>G	ENSP00000299697.9:p.Val176Gly
ENST00000417693.8:c.641T>G	ENSP00000407469.5:p.Val214Gly
ENST00000451102.7:c.602T>G	ENSP00000414334.4:p.Val201Gly
ENST00000527284.6:c.563-1669T>G
ENST00000527800.6:c.404T>G	ENSP00000433770.1:p.Val135Gly
ENST00000544898.6:c.695T>G MANE Select	ENSP00000440898.2:p.Val232Gly
ENST00000567357.6:c.*553T>G	ENSP00000457959.2:n.*553T>G
ENST00000569718.6:c.433T>G	ENSP00000464313.2:p.Phe145Val
ENST00000620035.5:c.451T>G	ENSP00000483833.2:p.Phe151Val
ENST00000676538.1:c.278T>G
ENST00000676904.1:c.166T>G
ENST00000677296.1:n.77T>G
ENST00000677379.1:c.336T>G	ENSP00000503672.1:n.336T>G
ENST00000677420.1:c.404T>G	ENSP00000504648.1:p.Val135Gly
ENST00000677555.1:c.404T>G	ENSP00000503331.1:p.Val135Gly
ENST00000677715.1:c.404T>G	ENSP00000502950.1:p.Val135Gly
ENST00000677753.1:n.77T>G
ENST00000677961.1:n.107T>G
ENST00000678015.1:c.404T>G	ENSP00000502959.1:p.Val135Gly
ENST00000678190.1:c.77T>G	ENSP00000503824.1:p.Val26Gly
ENST00000678282.1:n.77T>G
ENST00000678297.1:c.404T>G	ENSP00000503472.1:p.Val135Gly
ENST00000299697.11:c.695T>G	ENSP00000299697.8:p.Val232Gly
ENST00000417693.7:c.767T>G	ENSP00000407469.4:p.Val256Gly
ENST00000451102.6:c.821T>G	ENSP00000414334.3:p.Val274Gly
ENST00000525974.5:c.404T>G	ENSP00000434594.1:p.Val135Gly
ENST00000527284.5:c.602T>G	ENSP00000435312.1:p.Val201Gly
ENST00000527800.5:c.404T>G	ENSP00000433770.1:p.Val135Gly
ENST00000544898.5:c.695T>G	ENSP00000440898.2:p.Val232Gly
ENST00000545043.6:c.620T>G	ENSP00000438143.2:p.Val207Gly
ENST00000561527.5:n.254T>G
ENST00000561728.1:c.144T>G
ENST00000561905.2:c.49T>G
ENST00000562552.5:n.511T>G
ENST00000563099.5:n.222T>G
ENST00000563369.6:c.404T>G	ENSP00000463560.1:p.Val135Gly
ENST00000564792.1:n.350T>G
ENST00000564917.5:c.746T>G	ENSP00000455187.1:p.Val249Gly
ENST00000567357.5:c.*553T>G	ENSP00000457959.1:n.*553T>G
ENST00000569718.5:c.420T>G
ENST00000620035.4:c.641T>G	ENSP00000483833.1:p.Val214Gly
NM_001172643.1:c.602T>G	NP_001166114.1:p.Val201Gly
NM_001172644.1:c.620T>G	NP_001166115.1:p.Val207Gly
NM_001172645.1:c.641T>G	NP_001166116.1:p.Val214Gly
NM_001271934.1:c.548T>G	NP_001258863.1:p.Val183Gly
NM_001271935.1:c.433T>G	NP_001258864.1:p.Phe145Val
NM_001272050.1:c.404T>G	NP_001258979.1:p.Val135Gly
NM_004614.4:c.695T>G	NP_004605.4:p.Val232Gly
NR_073520.1:n.1974T>G
NM_001172644.2:c.620T>G	NP_001166115.1:p.Val207Gly
NM_001271934.2:c.548T>G	NP_001258863.1:p.Val183Gly
NM_001272050.2:c.404T>G	NP_001258979.1:p.Val135Gly
NM_004614.5:c.695T>G MANE Select	NP_004605.4:p.Val232Gly
NR_073520.2:n.1684T>G
NM_001172645.2:c.641T>G	NP_001166116.1:p.Val214Gly