Canonical Allele Identifier: CA396187139

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547666C>A (hg19) ; chr16:g.66513763C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513763C>A , CM000678.2:g.66513763C>A	GRCh38
NC_000016.9:g.66547666C>A , CM000678.1:g.66547666C>A	GRCh37
NC_000016.8:g.65105167C>A	NCBI36
NG_016862.1:g.41650G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.499G>T	ENSP00000299697.9:p.Gly167Cys
ENST00000417693.8:c.613G>T	ENSP00000407469.5:p.Gly205Cys
ENST00000451102.7:c.574G>T	ENSP00000414334.4:p.Gly192Cys
ENST00000527284.6:c.563-1697G>T
ENST00000527800.6:c.376G>T	ENSP00000433770.1:p.Gly126Cys
ENST00000544898.6:c.667G>T MANE Select	ENSP00000440898.2:p.Gly223Cys
ENST00000567357.6:c.*525G>T	ENSP00000457959.2:n.*525G>T
ENST00000569718.6:c.405G>T	ENSP00000464313.2:p.Lys135Asn
ENST00000620035.5:c.423G>T	ENSP00000483833.2:p.Lys141Asn
ENST00000676538.1:c.250G>T
ENST00000676904.1:c.138G>T
ENST00000677296.1:n.49G>T
ENST00000677379.1:c.308G>T	ENSP00000503672.1:n.308G>T
ENST00000677420.1:c.376G>T	ENSP00000504648.1:p.Gly126Cys
ENST00000677555.1:c.376G>T	ENSP00000503331.1:p.Gly126Cys
ENST00000677715.1:c.376G>T	ENSP00000502950.1:p.Gly126Cys
ENST00000677753.1:n.49G>T
ENST00000677961.1:n.79G>T
ENST00000678015.1:c.376G>T	ENSP00000502959.1:p.Gly126Cys
ENST00000678190.1:c.49G>T	ENSP00000503824.1:p.Gly17Cys
ENST00000678282.1:n.49G>T
ENST00000678297.1:c.376G>T	ENSP00000503472.1:p.Gly126Cys
ENST00000299697.11:c.667G>T	ENSP00000299697.8:p.Gly223Cys
ENST00000417693.7:c.739G>T	ENSP00000407469.4:p.Gly247Cys
ENST00000451102.6:c.793G>T	ENSP00000414334.3:p.Gly265Cys
ENST00000525974.5:c.376G>T	ENSP00000434594.1:p.Gly126Cys
ENST00000527284.5:c.574G>T	ENSP00000435312.1:p.Gly192Cys
ENST00000527800.5:c.376G>T	ENSP00000433770.1:p.Gly126Cys
ENST00000544898.5:c.667G>T	ENSP00000440898.2:p.Gly223Cys
ENST00000545043.6:c.592G>T	ENSP00000438143.2:p.Gly198Cys
ENST00000561527.5:n.226G>T
ENST00000561728.1:c.116G>T
ENST00000561905.2:c.21G>T
ENST00000562552.5:n.483G>T
ENST00000563099.5:n.194G>T
ENST00000563369.6:c.376G>T	ENSP00000463560.1:p.Gly126Cys
ENST00000563478.5:c.376G>T	ENSP00000462341.1:p.Gly126Cys
ENST00000564792.1:n.322G>T
ENST00000564917.5:c.718G>T	ENSP00000455187.1:p.Gly240Cys
ENST00000567357.5:c.*525G>T	ENSP00000457959.1:n.*525G>T
ENST00000569718.5:c.392G>T
ENST00000620035.4:c.613G>T	ENSP00000483833.1:p.Gly205Cys
NM_001172643.1:c.574G>T	NP_001166114.1:p.Gly192Cys
NM_001172644.1:c.592G>T	NP_001166115.1:p.Gly198Cys
NM_001172645.1:c.613G>T	NP_001166116.1:p.Gly205Cys
NM_001271934.1:c.520G>T	NP_001258863.1:p.Gly174Cys
NM_001271935.1:c.405G>T	NP_001258864.1:p.Lys135Asn
NM_001272050.1:c.376G>T	NP_001258979.1:p.Gly126Cys
NM_004614.4:c.667G>T	NP_004605.4:p.Gly223Cys
NR_073520.1:n.1946G>T
NM_001172644.2:c.592G>T	NP_001166115.1:p.Gly198Cys
NM_001271934.2:c.520G>T	NP_001258863.1:p.Gly174Cys
NM_001272050.2:c.376G>T	NP_001258979.1:p.Gly126Cys
NM_004614.5:c.667G>T MANE Select	NP_004605.4:p.Gly223Cys
NR_073520.2:n.1656G>T
NM_001172645.2:c.613G>T	NP_001166116.1:p.Gly205Cys