Canonical Allele Identifier: CA2228896302

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513779C= , CM000678.2:g.66513779C=	GRCh38
NC_000016.9:g.66547682C= , CM000678.1:g.66547682C=	GRCh37
NC_000016.8:g.65105183C=	NCBI36
NG_016862.1:g.41634G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.483G=	ENSP00000299697.9:p.Glu161=
ENST00000417693.8:c.597G=	ENSP00000407469.5:p.Glu199=
ENST00000451102.7:c.558G=	ENSP00000414334.4:p.Glu186=
ENST00000527284.6:c.563-1713G=
ENST00000527800.6:c.360G=	ENSP00000433770.1:p.Glu120=
ENST00000544898.6:c.651G= MANE Select	ENSP00000440898.2:p.Glu217=
ENST00000567357.6:c.*509G=	ENSP00000457959.2:n.*509G=
ENST00000569718.6:c.389G=	ENSP00000464313.2:p.Arg130=
ENST00000620035.5:c.407G=	ENSP00000483833.2:p.Arg136=
ENST00000676538.1:c.234G=
ENST00000676904.1:c.122G=
ENST00000677296.1:n.33G=
ENST00000677379.1:c.292G=	ENSP00000503672.1:n.292G=
ENST00000677420.1:c.360G=	ENSP00000504648.1:p.Glu120=
ENST00000677555.1:c.360G=	ENSP00000503331.1:p.Glu120=
ENST00000677715.1:c.360G=	ENSP00000502950.1:p.Glu120=
ENST00000677753.1:n.33G=
ENST00000677961.1:n.63G=
ENST00000678015.1:c.360G=	ENSP00000502959.1:p.Glu120=
ENST00000678190.1:c.33G=	ENSP00000503824.1:p.Glu11=
ENST00000678282.1:n.33G=
ENST00000678297.1:c.360G=	ENSP00000503472.1:p.Glu120=
ENST00000299697.11:c.651G=	ENSP00000299697.8:p.Glu217=
ENST00000417693.7:c.723G=	ENSP00000407469.4:p.Glu241=
ENST00000451102.6:c.777G=	ENSP00000414334.3:p.Glu259=
ENST00000525974.5:c.360G=	ENSP00000434594.1:p.Glu120=
ENST00000527284.5:c.558G=	ENSP00000435312.1:p.Glu186=
ENST00000527800.5:c.360G=	ENSP00000433770.1:p.Glu120=
ENST00000544898.5:c.651G=	ENSP00000440898.2:p.Glu217=
ENST00000545043.6:c.576G=	ENSP00000438143.2:p.Glu192=
ENST00000561527.5:n.210G=
ENST00000561728.1:c.100G=
ENST00000561905.2:c.5G=
ENST00000562552.5:n.467G=
ENST00000563099.5:n.178G=
ENST00000563369.6:c.360G=	ENSP00000463560.1:p.Glu120=
ENST00000563478.5:c.360G=	ENSP00000462341.1:p.Glu120=
ENST00000564792.1:n.306G=
ENST00000564917.5:c.702G=	ENSP00000455187.1:p.Glu234=
ENST00000567357.5:c.*509G=	ENSP00000457959.1:n.*509G=
ENST00000569718.5:c.376G=
ENST00000620035.4:c.597G=	ENSP00000483833.1:p.Glu199=
NM_001172643.1:c.558G=	NP_001166114.1:p.Glu186=
NM_001172644.1:c.576G=	NP_001166115.1:p.Glu192=
NM_001172645.1:c.597G=	NP_001166116.1:p.Glu199=
NM_001271934.1:c.504G=	NP_001258863.1:p.Glu168=
NM_001271935.1:c.389G=	NP_001258864.1:p.Arg130=
NM_001272050.1:c.360G=	NP_001258979.1:p.Glu120=
NM_004614.4:c.651G=	NP_004605.4:p.Glu217=
NR_073520.1:n.1930G=
NM_001172644.2:c.576G=	NP_001166115.1:p.Glu192=
NM_001271934.2:c.504G=	NP_001258863.1:p.Glu168=
NM_001272050.2:c.360G=	NP_001258979.1:p.Glu120=
NM_004614.5:c.651G= MANE Select	NP_004605.4:p.Glu217=
NR_073520.2:n.1640G=
NM_001172645.2:c.597G=	NP_001166116.1:p.Glu199=