Canonical Allele Identifier: CA396187352

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513807T>C , CM000678.2:g.66513807T>C	GRCh38
NC_000016.9:g.66547710T>C , CM000678.1:g.66547710T>C	GRCh37
NC_000016.8:g.65105211T>C	NCBI36
NG_016862.1:g.41606A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004614.5:c.623A>G MANE Select	NP_004605.4:p.Tyr208Cys
ENST00000544898.6:c.623A>G MANE Select	ENSP00000440898.2:p.Tyr208Cys
NM_001172643.1:c.530A>G	NP_001166114.1:p.Tyr177Cys
NM_001172644.1:c.548A>G	NP_001166115.1:p.Tyr183Cys
NM_001172644.2:c.548A>G	NP_001166115.1:p.Tyr183Cys
NM_001172645.1:c.569A>G	NP_001166116.1:p.Tyr190Cys
NM_001172645.2:c.569A>G	NP_001166116.1:p.Tyr190Cys
NM_001271934.1:c.476A>G	NP_001258863.1:p.Tyr159Cys
NM_001271934.2:c.476A>G	NP_001258863.1:p.Tyr159Cys
NM_001271935.1:c.361A>G	NP_001258864.1:p.Thr121Ala
NM_001272050.1:c.332A>G	NP_001258979.1:p.Tyr111Cys
NM_001272050.2:c.332A>G	NP_001258979.1:p.Tyr111Cys
NM_004614.4:c.623A>G	NP_004605.4:p.Tyr208Cys
NR_073520.1:n.1902A>G
NR_073520.2:n.1612A>G
ENST00000299697.11:c.623A>G	ENSP00000299697.8:p.Tyr208Cys
ENST00000299697.12:c.455A>G	ENSP00000299697.9:p.Tyr152Cys
ENST00000417693.7:c.695A>G	ENSP00000407469.4:p.Tyr232Cys
ENST00000417693.8:c.569A>G	ENSP00000407469.5:p.Tyr190Cys
ENST00000451102.6:c.749A>G	ENSP00000414334.3:p.Tyr250Cys
ENST00000451102.7:c.530A>G	ENSP00000414334.4:p.Tyr177Cys
ENST00000525974.5:c.332A>G	ENSP00000434594.1:p.Tyr111Cys
ENST00000527284.5:c.530A>G	ENSP00000435312.1:p.Tyr177Cys
ENST00000527284.6:c.563-1741A>G
ENST00000527800.5:c.332A>G	ENSP00000433770.1:p.Tyr111Cys
ENST00000527800.6:c.332A>G	ENSP00000433770.1:p.Tyr111Cys
ENST00000544898.5:c.623A>G	ENSP00000440898.2:p.Tyr208Cys
ENST00000545043.6:c.548A>G	ENSP00000438143.2:p.Tyr183Cys
ENST00000561527.5:n.182A>G
ENST00000561728.1:c.72A>G
ENST00000562552.5:n.439A>G
ENST00000563099.5:n.150A>G
ENST00000563369.6:c.332A>G	ENSP00000463560.1:p.Tyr111Cys
ENST00000563478.5:c.332A>G	ENSP00000462341.1:p.Tyr111Cys
ENST00000564792.1:n.278A>G
ENST00000564917.5:c.674A>G	ENSP00000455187.1:p.Tyr225Cys
ENST00000567357.5:c.*481A>G	ENSP00000457959.1:n.*481A>G
ENST00000567357.6:c.*481A>G	ENSP00000457959.2:n.*481A>G
ENST00000569718.5:c.348A>G
ENST00000569718.6:c.361A>G	ENSP00000464313.2:p.Thr121Ala
ENST00000620035.4:c.569A>G	ENSP00000483833.1:p.Tyr190Cys
ENST00000620035.5:c.379A>G	ENSP00000483833.2:p.Thr127Ala
ENST00000676538.1:c.206A>G
ENST00000676904.1:c.94A>G
ENST00000677296.1:n.5A>G
ENST00000677379.1:c.264A>G	ENSP00000503672.1:n.264A>G
ENST00000677420.1:c.332A>G	ENSP00000504648.1:p.Tyr111Cys
ENST00000677555.1:c.332A>G	ENSP00000503331.1:p.Tyr111Cys
ENST00000677715.1:c.332A>G	ENSP00000502950.1:p.Tyr111Cys
ENST00000677753.1:n.5A>G
ENST00000677961.1:n.35A>G
ENST00000678015.1:c.332A>G	ENSP00000502959.1:p.Tyr111Cys
ENST00000678190.1:c.5A>G	ENSP00000503824.1:p.Tyr2Cys
ENST00000678282.1:n.5A>G
ENST00000678297.1:c.332A>G	ENSP00000503472.1:p.Tyr111Cys