Canonical Allele Identifier: CA2228908927

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513750G= , CM000678.2:g.66513750G=	GRCh38
NC_000016.9:g.66547653G= , CM000678.1:g.66547653G=	GRCh37
NC_000016.8:g.65105154G=	NCBI36
NG_016862.1:g.41663C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.512C=	ENSP00000299697.9:p.Pro171=
ENST00000417693.8:c.626C=	ENSP00000407469.5:p.Pro209=
ENST00000451102.7:c.587C=	ENSP00000414334.4:p.Pro196=
ENST00000527284.6:c.563-1684C=
ENST00000527800.6:c.389C=	ENSP00000433770.1:p.Pro130=
ENST00000544898.6:c.680C= MANE Select	ENSP00000440898.2:p.Pro227=
ENST00000567357.6:c.*538C=	ENSP00000457959.2:n.*538C=
ENST00000569718.6:c.418C=	ENSP00000464313.2:p.Pro140=
ENST00000620035.5:c.436C=	ENSP00000483833.2:p.Pro146=
ENST00000676538.1:c.263C=
ENST00000676904.1:c.151C=
ENST00000677296.1:n.62C=
ENST00000677379.1:c.321C=	ENSP00000503672.1:n.321C=
ENST00000677420.1:c.389C=	ENSP00000504648.1:p.Pro130=
ENST00000677555.1:c.389C=	ENSP00000503331.1:p.Pro130=
ENST00000677715.1:c.389C=	ENSP00000502950.1:p.Pro130=
ENST00000677753.1:n.62C=
ENST00000677961.1:n.92C=
ENST00000678015.1:c.389C=	ENSP00000502959.1:p.Pro130=
ENST00000678190.1:c.62C=	ENSP00000503824.1:p.Pro21=
ENST00000678282.1:n.62C=
ENST00000678297.1:c.389C=	ENSP00000503472.1:p.Pro130=
ENST00000299697.11:c.680C=	ENSP00000299697.8:p.Pro227=
ENST00000417693.7:c.752C=	ENSP00000407469.4:p.Pro251=
ENST00000451102.6:c.806C=	ENSP00000414334.3:p.Pro269=
ENST00000525974.5:c.389C=	ENSP00000434594.1:p.Pro130=
ENST00000527284.5:c.587C=	ENSP00000435312.1:p.Pro196=
ENST00000527800.5:c.389C=	ENSP00000433770.1:p.Pro130=
ENST00000544898.5:c.680C=	ENSP00000440898.2:p.Pro227=
ENST00000545043.6:c.605C=	ENSP00000438143.2:p.Pro202=
ENST00000561527.5:n.239C=
ENST00000561728.1:c.129C=
ENST00000561905.2:c.34C=
ENST00000562552.5:n.496C=
ENST00000563099.5:n.207C=
ENST00000563369.6:c.389C=	ENSP00000463560.1:p.Pro130=
ENST00000563478.5:c.389C=	ENSP00000462341.1:p.Pro130=
ENST00000564792.1:n.335C=
ENST00000564917.5:c.731C=	ENSP00000455187.1:p.Pro244=
ENST00000567357.5:c.*538C=	ENSP00000457959.1:n.*538C=
ENST00000569718.5:c.405C=
ENST00000620035.4:c.626C=	ENSP00000483833.1:p.Pro209=
NM_001172643.1:c.587C=	NP_001166114.1:p.Pro196=
NM_001172644.1:c.605C=	NP_001166115.1:p.Pro202=
NM_001172645.1:c.626C=	NP_001166116.1:p.Pro209=
NM_001271934.1:c.533C=	NP_001258863.1:p.Pro178=
NM_001271935.1:c.418C=	NP_001258864.1:p.Pro140=
NM_001272050.1:c.389C=	NP_001258979.1:p.Pro130=
NM_004614.4:c.680C=	NP_004605.4:p.Pro227=
NR_073520.1:n.1959C=
NM_001172644.2:c.605C=	NP_001166115.1:p.Pro202=
NM_001271934.2:c.533C=	NP_001258863.1:p.Pro178=
NM_001272050.2:c.389C=	NP_001258979.1:p.Pro130=
NM_004614.5:c.680C= MANE Select	NP_004605.4:p.Pro227=
NR_073520.2:n.1669C=
NM_001172645.2:c.626C=	NP_001166116.1:p.Pro209=