Canonical Allele Identifier: CA495903004

Gene: TK2

Linked Data

• dbSNP Id: rs1964523081
• COSMIC: COSM5636063 ; COSM5636064
• MyVariant Identifiers: chr16:g.66547706C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513803C>T , CM000678.2:g.66513803C>T	GRCh38
NC_000016.9:g.66547706C>T , CM000678.1:g.66547706C>T	GRCh37
NC_000016.8:g.65105207C>T	NCBI36
NG_016862.1:g.41610G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.459G>A	ENSP00000299697.9:p.Leu153=
ENST00000417693.8:c.573G>A	ENSP00000407469.5:p.Leu191=
ENST00000451102.7:c.534G>A	ENSP00000414334.4:p.Leu178=
ENST00000527284.6:c.563-1737G>A
ENST00000527800.6:c.336G>A	ENSP00000433770.1:p.Leu112=
ENST00000544898.6:c.627G>A MANE Select	ENSP00000440898.2:p.Leu209=
ENST00000567357.6:c.*485G>A	ENSP00000457959.2:n.*485G>A
ENST00000569718.6:c.365G>A	ENSP00000464313.2:p.Trp122Ter
ENST00000620035.5:c.383G>A	ENSP00000483833.2:p.Trp128Ter
ENST00000676538.1:c.210G>A
ENST00000676904.1:c.98G>A
ENST00000677296.1:n.9G>A
ENST00000677379.1:c.268G>A	ENSP00000503672.1:n.268G>A
ENST00000677420.1:c.336G>A	ENSP00000504648.1:p.Leu112=
ENST00000677555.1:c.336G>A	ENSP00000503331.1:p.Leu112=
ENST00000677715.1:c.336G>A	ENSP00000502950.1:p.Leu112=
ENST00000677753.1:n.9G>A
ENST00000677961.1:n.39G>A
ENST00000678015.1:c.336G>A	ENSP00000502959.1:p.Leu112=
ENST00000678190.1:c.9G>A	ENSP00000503824.1:p.Leu3=
ENST00000678282.1:n.9G>A
ENST00000678297.1:c.336G>A	ENSP00000503472.1:p.Leu112=
ENST00000299697.11:c.627G>A	ENSP00000299697.8:p.Leu209=
ENST00000417693.7:c.699G>A	ENSP00000407469.4:p.Leu233=
ENST00000451102.6:c.753G>A	ENSP00000414334.3:p.Leu251=
ENST00000525974.5:c.336G>A	ENSP00000434594.1:p.Leu112=
ENST00000527284.5:c.534G>A	ENSP00000435312.1:p.Leu178=
ENST00000527800.5:c.336G>A	ENSP00000433770.1:p.Leu112=
ENST00000544898.5:c.627G>A	ENSP00000440898.2:p.Leu209=
ENST00000545043.6:c.552G>A	ENSP00000438143.2:p.Leu184=
ENST00000561527.5:n.186G>A
ENST00000561728.1:c.76G>A
ENST00000562552.5:n.443G>A
ENST00000563099.5:n.154G>A
ENST00000563369.6:c.336G>A	ENSP00000463560.1:p.Leu112=
ENST00000563478.5:c.336G>A	ENSP00000462341.1:p.Leu112=
ENST00000564792.1:n.282G>A
ENST00000564917.5:c.678G>A	ENSP00000455187.1:p.Leu226=
ENST00000567357.5:c.*485G>A	ENSP00000457959.1:n.*485G>A
ENST00000569718.5:c.352G>A
ENST00000620035.4:c.573G>A	ENSP00000483833.1:p.Leu191=
NM_001172643.1:c.534G>A	NP_001166114.1:p.Leu178=
NM_001172644.1:c.552G>A	NP_001166115.1:p.Leu184=
NM_001172645.1:c.573G>A	NP_001166116.1:p.Leu191=
NM_001271934.1:c.480G>A	NP_001258863.1:p.Leu160=
NM_001271935.1:c.365G>A	NP_001258864.1:p.Trp122Ter
NM_001272050.1:c.336G>A	NP_001258979.1:p.Leu112=
NM_004614.4:c.627G>A	NP_004605.4:p.Leu209=
NR_073520.1:n.1906G>A
NM_001172644.2:c.552G>A	NP_001166115.1:p.Leu184=
NM_001271934.2:c.480G>A	NP_001258863.1:p.Leu160=
NM_001272050.2:c.336G>A	NP_001258979.1:p.Leu112=
NM_004614.5:c.627G>A MANE Select	NP_004605.4:p.Leu209=
NR_073520.2:n.1616G>A
NM_001172645.2:c.573G>A	NP_001166116.1:p.Leu191=