Canonical Allele Identifier: CA2228908918

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513732A= , CM000678.2:g.66513732A=	GRCh38
NC_000016.9:g.66547635A= , CM000678.1:g.66547635A=	GRCh37
NC_000016.8:g.65105136A=	NCBI36
NG_016862.1:g.41681T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.530T=	ENSP00000299697.9:p.Leu177=
ENST00000417693.8:c.644T=	ENSP00000407469.5:p.Leu215=
ENST00000451102.7:c.605T=	ENSP00000414334.4:p.Leu202=
ENST00000527284.6:c.563-1666T=
ENST00000527800.6:c.407T=	ENSP00000433770.1:p.Leu136=
ENST00000544898.6:c.698T= MANE Select	ENSP00000440898.2:p.Leu233=
ENST00000567357.6:c.*556T=	ENSP00000457959.2:n.*556T=
ENST00000569718.6:c.436T=	ENSP00000464313.2:p.Trp146=
ENST00000620035.5:c.454T=	ENSP00000483833.2:p.Trp152=
ENST00000676538.1:c.281T=
ENST00000676904.1:c.169T=
ENST00000677296.1:n.80T=
ENST00000677379.1:c.339T=	ENSP00000503672.1:n.339T=
ENST00000677420.1:c.407T=	ENSP00000504648.1:p.Leu136=
ENST00000677555.1:c.407T=	ENSP00000503331.1:p.Leu136=
ENST00000677715.1:c.407T=	ENSP00000502950.1:p.Leu136=
ENST00000677753.1:n.80T=
ENST00000677961.1:n.110T=
ENST00000678015.1:c.407T=	ENSP00000502959.1:p.Leu136=
ENST00000678190.1:c.80T=	ENSP00000503824.1:p.Leu27=
ENST00000678282.1:n.80T=
ENST00000678297.1:c.407T=	ENSP00000503472.1:p.Leu136=
ENST00000299697.11:c.698T=	ENSP00000299697.8:p.Leu233=
ENST00000417693.7:c.770T=	ENSP00000407469.4:p.Leu257=
ENST00000451102.6:c.824T=	ENSP00000414334.3:p.Leu275=
ENST00000525974.5:c.407T=	ENSP00000434594.1:p.Leu136=
ENST00000527284.5:c.605T=	ENSP00000435312.1:p.Leu202=
ENST00000527800.5:c.407T=	ENSP00000433770.1:p.Leu136=
ENST00000544898.5:c.698T=	ENSP00000440898.2:p.Leu233=
ENST00000545043.6:c.623T=	ENSP00000438143.2:p.Leu208=
ENST00000561527.5:n.257T=
ENST00000561728.1:c.147T=
ENST00000561905.2:c.52T=
ENST00000562552.5:n.514T=
ENST00000563099.5:n.225T=
ENST00000563369.6:c.407T=	ENSP00000463560.1:p.Leu136=
ENST00000564792.1:n.353T=
ENST00000564917.5:c.749T=	ENSP00000455187.1:p.Leu250=
ENST00000567357.5:c.*556T=	ENSP00000457959.1:n.*556T=
ENST00000569718.5:c.423T=
ENST00000620035.4:c.644T=	ENSP00000483833.1:p.Leu215=
NM_001172643.1:c.605T=	NP_001166114.1:p.Leu202=
NM_001172644.1:c.623T=	NP_001166115.1:p.Leu208=
NM_001172645.1:c.644T=	NP_001166116.1:p.Leu215=
NM_001271934.1:c.551T=	NP_001258863.1:p.Leu184=
NM_001271935.1:c.436T=	NP_001258864.1:p.Trp146=
NM_001272050.1:c.407T=	NP_001258979.1:p.Leu136=
NM_004614.4:c.698T=	NP_004605.4:p.Leu233=
NR_073520.1:n.1977T=
NM_001172644.2:c.623T=	NP_001166115.1:p.Leu208=
NM_001271934.2:c.551T=	NP_001258863.1:p.Leu184=
NM_001272050.2:c.407T=	NP_001258979.1:p.Leu136=
NM_004614.5:c.698T= MANE Select	NP_004605.4:p.Leu233=
NR_073520.2:n.1687T=
NM_001172645.2:c.644T=	NP_001166116.1:p.Leu215=