Canonical Allele Identifier: CA396187278

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547693G>C (hg19) ; chr16:g.66513790G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513790G>C , CM000678.2:g.66513790G>C	GRCh38
NC_000016.9:g.66547693G>C , CM000678.1:g.66547693G>C	GRCh37
NC_000016.8:g.65105194G>C	NCBI36
NG_016862.1:g.41623C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.472C>G	ENSP00000299697.9:p.His158Asp
ENST00000417693.8:c.586C>G	ENSP00000407469.5:p.His196Asp
ENST00000451102.7:c.547C>G	ENSP00000414334.4:p.His183Asp
ENST00000527284.6:c.563-1724C>G
ENST00000527800.6:c.349C>G	ENSP00000433770.1:p.His117Asp
ENST00000544898.6:c.640C>G MANE Select	ENSP00000440898.2:p.His214Asp
ENST00000567357.6:c.*498C>G	ENSP00000457959.2:n.*498C>G
ENST00000569718.6:c.378C>G	ENSP00000464313.2:p.Thr126=
ENST00000620035.5:c.396C>G	ENSP00000483833.2:p.Thr132=
ENST00000676538.1:c.223C>G
ENST00000676904.1:c.111C>G
ENST00000677296.1:n.22C>G
ENST00000677379.1:c.281C>G	ENSP00000503672.1:n.281C>G
ENST00000677420.1:c.349C>G	ENSP00000504648.1:p.His117Asp
ENST00000677555.1:c.349C>G	ENSP00000503331.1:p.His117Asp
ENST00000677715.1:c.349C>G	ENSP00000502950.1:p.His117Asp
ENST00000677753.1:n.22C>G
ENST00000677961.1:n.52C>G
ENST00000678015.1:c.349C>G	ENSP00000502959.1:p.His117Asp
ENST00000678190.1:c.22C>G	ENSP00000503824.1:p.His8Asp
ENST00000678282.1:n.22C>G
ENST00000678297.1:c.349C>G	ENSP00000503472.1:p.His117Asp
ENST00000299697.11:c.640C>G	ENSP00000299697.8:p.His214Asp
ENST00000417693.7:c.712C>G	ENSP00000407469.4:p.His238Asp
ENST00000451102.6:c.766C>G	ENSP00000414334.3:p.His256Asp
ENST00000525974.5:c.349C>G	ENSP00000434594.1:p.His117Asp
ENST00000527284.5:c.547C>G	ENSP00000435312.1:p.His183Asp
ENST00000527800.5:c.349C>G	ENSP00000433770.1:p.His117Asp
ENST00000544898.5:c.640C>G	ENSP00000440898.2:p.His214Asp
ENST00000545043.6:c.565C>G	ENSP00000438143.2:p.His189Asp
ENST00000561527.5:n.199C>G
ENST00000561728.1:c.89C>G
ENST00000562552.5:n.456C>G
ENST00000563099.5:n.167C>G
ENST00000563369.6:c.349C>G	ENSP00000463560.1:p.His117Asp
ENST00000563478.5:c.349C>G	ENSP00000462341.1:p.His117Asp
ENST00000564792.1:n.295C>G
ENST00000564917.5:c.691C>G	ENSP00000455187.1:p.His231Asp
ENST00000567357.5:c.*498C>G	ENSP00000457959.1:n.*498C>G
ENST00000569718.5:c.365C>G
ENST00000620035.4:c.586C>G	ENSP00000483833.1:p.His196Asp
NM_001172643.1:c.547C>G	NP_001166114.1:p.His183Asp
NM_001172644.1:c.565C>G	NP_001166115.1:p.His189Asp
NM_001172645.1:c.586C>G	NP_001166116.1:p.His196Asp
NM_001271934.1:c.493C>G	NP_001258863.1:p.His165Asp
NM_001271935.1:c.378C>G	NP_001258864.1:p.Thr126=
NM_001272050.1:c.349C>G	NP_001258979.1:p.His117Asp
NM_004614.4:c.640C>G	NP_004605.4:p.His214Asp
NR_073520.1:n.1919C>G
NM_001172644.2:c.565C>G	NP_001166115.1:p.His189Asp
NM_001271934.2:c.493C>G	NP_001258863.1:p.His165Asp
NM_001272050.2:c.349C>G	NP_001258979.1:p.His117Asp
NM_004614.5:c.640C>G MANE Select	NP_004605.4:p.His214Asp
NR_073520.2:n.1629C>G
NM_001172645.2:c.586C>G	NP_001166116.1:p.His196Asp