Canonical Allele Identifier: CA396187214

Gene: TK2

Linked Data

• COSMIC: COSM3988570 ; COSM3988571
• MyVariant Identifiers: chr16:g.66547680T>A (hg19) ; chr16:g.66513777T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513777T>A , CM000678.2:g.66513777T>A	GRCh38
NC_000016.9:g.66547680T>A , CM000678.1:g.66547680T>A	GRCh37
NC_000016.8:g.65105181T>A	NCBI36
NG_016862.1:g.41636A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.485A>T	ENSP00000299697.9:p.Glu162Val
ENST00000417693.8:c.599A>T	ENSP00000407469.5:p.Glu200Val
ENST00000451102.7:c.560A>T	ENSP00000414334.4:p.Glu187Val
ENST00000527284.6:c.563-1711A>T
ENST00000527800.6:c.362A>T	ENSP00000433770.1:p.Glu121Val
ENST00000544898.6:c.653A>T MANE Select	ENSP00000440898.2:p.Glu218Val
ENST00000567357.6:c.*511A>T	ENSP00000457959.2:n.*511A>T
ENST00000569718.6:c.391A>T	ENSP00000464313.2:p.Ser131Cys
ENST00000620035.5:c.409A>T	ENSP00000483833.2:p.Ser137Cys
ENST00000676538.1:c.236A>T
ENST00000676904.1:c.124A>T
ENST00000677296.1:n.35A>T
ENST00000677379.1:c.294A>T	ENSP00000503672.1:n.294A>T
ENST00000677420.1:c.362A>T	ENSP00000504648.1:p.Glu121Val
ENST00000677555.1:c.362A>T	ENSP00000503331.1:p.Glu121Val
ENST00000677715.1:c.362A>T	ENSP00000502950.1:p.Glu121Val
ENST00000677753.1:n.35A>T
ENST00000677961.1:n.65A>T
ENST00000678015.1:c.362A>T	ENSP00000502959.1:p.Glu121Val
ENST00000678190.1:c.35A>T	ENSP00000503824.1:p.Glu12Val
ENST00000678282.1:n.35A>T
ENST00000678297.1:c.362A>T	ENSP00000503472.1:p.Glu121Val
ENST00000299697.11:c.653A>T	ENSP00000299697.8:p.Glu218Val
ENST00000417693.7:c.725A>T	ENSP00000407469.4:p.Glu242Val
ENST00000451102.6:c.779A>T	ENSP00000414334.3:p.Glu260Val
ENST00000525974.5:c.362A>T	ENSP00000434594.1:p.Glu121Val
ENST00000527284.5:c.560A>T	ENSP00000435312.1:p.Glu187Val
ENST00000527800.5:c.362A>T	ENSP00000433770.1:p.Glu121Val
ENST00000544898.5:c.653A>T	ENSP00000440898.2:p.Glu218Val
ENST00000545043.6:c.578A>T	ENSP00000438143.2:p.Glu193Val
ENST00000561527.5:n.212A>T
ENST00000561728.1:c.102A>T
ENST00000561905.2:c.7A>T
ENST00000562552.5:n.469A>T
ENST00000563099.5:n.180A>T
ENST00000563369.6:c.362A>T	ENSP00000463560.1:p.Glu121Val
ENST00000563478.5:c.362A>T	ENSP00000462341.1:p.Glu121Val
ENST00000564792.1:n.308A>T
ENST00000564917.5:c.704A>T	ENSP00000455187.1:p.Glu235Val
ENST00000567357.5:c.*511A>T	ENSP00000457959.1:n.*511A>T
ENST00000569718.5:c.378A>T
ENST00000620035.4:c.599A>T	ENSP00000483833.1:p.Glu200Val
NM_001172643.1:c.560A>T	NP_001166114.1:p.Glu187Val
NM_001172644.1:c.578A>T	NP_001166115.1:p.Glu193Val
NM_001172645.1:c.599A>T	NP_001166116.1:p.Glu200Val
NM_001271934.1:c.506A>T	NP_001258863.1:p.Glu169Val
NM_001271935.1:c.391A>T	NP_001258864.1:p.Ser131Cys
NM_001272050.1:c.362A>T	NP_001258979.1:p.Glu121Val
NM_004614.4:c.653A>T	NP_004605.4:p.Glu218Val
NR_073520.1:n.1932A>T
NM_001172644.2:c.578A>T	NP_001166115.1:p.Glu193Val
NM_001271934.2:c.506A>T	NP_001258863.1:p.Glu169Val
NM_001272050.2:c.362A>T	NP_001258979.1:p.Glu121Val
NM_004614.5:c.653A>T MANE Select	NP_004605.4:p.Glu218Val
NR_073520.2:n.1642A>T
NM_001172645.2:c.599A>T	NP_001166116.1:p.Glu200Val