Canonical Allele Identifier: CA343315

Gene: TK2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66517179C>T , CM000678.2:g.66517179C>T	GRCh38
NC_000016.9:g.66551082C>T , CM000678.1:g.66551082C>T	GRCh37
NC_000016.8:g.65108583C>T	NCBI36
NG_016862.1:g.38234G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.407G>A	ENSP00000299697.9:p.Arg136Lys
ENST00000417693.8:c.521G>A	ENSP00000407469.5:p.Arg174Lys
ENST00000451102.7:c.482G>A	ENSP00000414334.4:p.Arg161Lys
ENST00000527284.6:c.519G>A
ENST00000527800.6:c.284G>A	ENSP00000433770.1:p.Arg95Lys
ENST00000544898.6:c.575G>A MANE Select	ENSP00000440898.2:p.Arg192Lys
ENST00000567357.6:c.*433G>A	ENSP00000457959.2:n.*433G>A
ENST00000569718.6:c.357-3368G>A	ENSP00000464313.2:n.357-3368G>A
ENST00000620035.5:c.375-3368G>A	ENSP00000483833.2:n.375-3368G>A
ENST00000676538.1:c.158G>A
ENST00000676904.1:c.89+610G>A
ENST00000677379.1:c.216G>A	ENSP00000503672.1:n.216G>A
ENST00000677420.1:c.284G>A	ENSP00000504648.1:p.Arg95Lys
ENST00000677555.1:c.284G>A	ENSP00000503331.1:p.Arg95Lys
ENST00000677715.1:c.284G>A	ENSP00000502950.1:p.Arg95Lys
ENST00000678015.1:c.284G>A	ENSP00000502959.1:p.Arg95Lys
ENST00000678297.1:c.284G>A	ENSP00000503472.1:p.Arg95Lys
ENST00000678314.1:c.284G>A	ENSP00000504438.1:p.Arg95Lys
ENST00000299697.11:c.575G>A	ENSP00000299697.8:p.Arg192Lys
ENST00000417693.7:c.647G>A	ENSP00000407469.4:p.Arg216Lys
ENST00000451102.6:c.701G>A	ENSP00000414334.3:p.Arg234Lys
ENST00000525974.5:c.284G>A	ENSP00000434594.1:p.Arg95Lys
ENST00000527284.5:c.482G>A	ENSP00000435312.1:p.Arg161Lys
ENST00000527800.5:c.284G>A	ENSP00000433770.1:p.Arg95Lys
ENST00000544898.5:c.575G>A	ENSP00000440898.2:p.Arg192Lys
ENST00000545043.6:c.500G>A	ENSP00000438143.2:p.Arg167Lys
ENST00000561527.5:n.134G>A
ENST00000561728.1:c.24G>A
ENST00000562552.5:n.391G>A
ENST00000563099.5:n.102G>A
ENST00000563369.6:c.284G>A	ENSP00000463560.1:p.Arg95Lys
ENST00000563478.5:c.284G>A	ENSP00000462341.1:p.Arg95Lys
ENST00000564792.1:n.230G>A
ENST00000564917.5:c.575G>A	ENSP00000455187.1:p.Arg192Lys
ENST00000567357.5:c.*433G>A	ENSP00000457959.1:n.*433G>A
ENST00000569718.5:c.344-3368G>A
ENST00000620035.4:c.521G>A	ENSP00000483833.1:p.Arg174Lys
NM_001172643.1:c.482G>A	NP_001166114.1:p.Arg161Lys
NM_001172644.1:c.500G>A	NP_001166115.1:p.Arg167Lys
NM_001172645.1:c.521G>A	NP_001166116.1:p.Arg174Lys
NM_001271934.1:c.428G>A	NP_001258863.1:p.Arg143Lys
NM_001271935.1:c.357-3368G>A	NP_001258864.1:n.357-3368G>A
NM_001272050.1:c.284G>A	NP_001258979.1:p.Arg95Lys
NM_004614.4:c.575G>A	NP_004605.4:p.Arg192Lys
NR_073520.1:n.1854G>A
NM_001172644.2:c.500G>A	NP_001166115.1:p.Arg167Lys
NM_001271934.2:c.428G>A	NP_001258863.1:p.Arg143Lys
NM_001272050.2:c.284G>A	NP_001258979.1:p.Arg95Lys
NM_004614.5:c.575G>A MANE Select	NP_004605.4:p.Arg192Lys
NR_073520.2:n.1564G>A
NM_001172645.2:c.521G>A	NP_001166116.1:p.Arg174Lys