Canonical Allele Identifier: CA495902924

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547637A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513734A>C , CM000678.2:g.66513734A>C	GRCh38
NC_000016.9:g.66547637A>C , CM000678.1:g.66547637A>C	GRCh37
NC_000016.8:g.65105138A>C	NCBI36
NG_016862.1:g.41679T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.528T>G	ENSP00000299697.9:p.Val176=
ENST00000417693.8:c.642T>G	ENSP00000407469.5:p.Val214=
ENST00000451102.7:c.603T>G	ENSP00000414334.4:p.Val201=
ENST00000527284.6:c.563-1668T>G
ENST00000527800.6:c.405T>G	ENSP00000433770.1:p.Val135=
ENST00000544898.6:c.696T>G MANE Select	ENSP00000440898.2:p.Val232=
ENST00000567357.6:c.*554T>G	ENSP00000457959.2:n.*554T>G
ENST00000569718.6:c.434T>G	ENSP00000464313.2:p.Phe145Cys
ENST00000620035.5:c.452T>G	ENSP00000483833.2:p.Phe151Cys
ENST00000676538.1:c.279T>G
ENST00000676904.1:c.167T>G
ENST00000677296.1:n.78T>G
ENST00000677379.1:c.337T>G	ENSP00000503672.1:n.337T>G
ENST00000677420.1:c.405T>G	ENSP00000504648.1:p.Val135=
ENST00000677555.1:c.405T>G	ENSP00000503331.1:p.Val135=
ENST00000677715.1:c.405T>G	ENSP00000502950.1:p.Val135=
ENST00000677753.1:n.78T>G
ENST00000677961.1:n.108T>G
ENST00000678015.1:c.405T>G	ENSP00000502959.1:p.Val135=
ENST00000678190.1:c.78T>G	ENSP00000503824.1:p.Val26=
ENST00000678282.1:n.78T>G
ENST00000678297.1:c.405T>G	ENSP00000503472.1:p.Val135=
ENST00000299697.11:c.696T>G	ENSP00000299697.8:p.Val232=
ENST00000417693.7:c.768T>G	ENSP00000407469.4:p.Val256=
ENST00000451102.6:c.822T>G	ENSP00000414334.3:p.Val274=
ENST00000525974.5:c.405T>G	ENSP00000434594.1:p.Val135=
ENST00000527284.5:c.603T>G	ENSP00000435312.1:p.Val201=
ENST00000527800.5:c.405T>G	ENSP00000433770.1:p.Val135=
ENST00000544898.5:c.696T>G	ENSP00000440898.2:p.Val232=
ENST00000545043.6:c.621T>G	ENSP00000438143.2:p.Val207=
ENST00000561527.5:n.255T>G
ENST00000561728.1:c.145T>G
ENST00000561905.2:c.50T>G
ENST00000562552.5:n.512T>G
ENST00000563099.5:n.223T>G
ENST00000563369.6:c.405T>G	ENSP00000463560.1:p.Val135=
ENST00000564792.1:n.351T>G
ENST00000564917.5:c.747T>G	ENSP00000455187.1:p.Val249=
ENST00000567357.5:c.*554T>G	ENSP00000457959.1:n.*554T>G
ENST00000569718.5:c.421T>G
ENST00000620035.4:c.642T>G	ENSP00000483833.1:p.Val214=
NM_001172643.1:c.603T>G	NP_001166114.1:p.Val201=
NM_001172644.1:c.621T>G	NP_001166115.1:p.Val207=
NM_001172645.1:c.642T>G	NP_001166116.1:p.Val214=
NM_001271934.1:c.549T>G	NP_001258863.1:p.Val183=
NM_001271935.1:c.434T>G	NP_001258864.1:p.Phe145Cys
NM_001272050.1:c.405T>G	NP_001258979.1:p.Val135=
NM_004614.4:c.696T>G	NP_004605.4:p.Val232=
NR_073520.1:n.1975T>G
NM_001172644.2:c.621T>G	NP_001166115.1:p.Val207=
NM_001271934.2:c.549T>G	NP_001258863.1:p.Val183=
NM_001272050.2:c.405T>G	NP_001258979.1:p.Val135=
NM_004614.5:c.696T>G MANE Select	NP_004605.4:p.Val232=
NR_073520.2:n.1685T>G
NM_001172645.2:c.642T>G	NP_001166116.1:p.Val214=