Canonical Allele Identifier: CA396190631

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66565338A>T (hg19) ; chr16:g.66531435A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531435A>T , CM000678.2:g.66531435A>T	GRCh38
NC_000016.9:g.66565338A>T , CM000678.1:g.66565338A>T	GRCh37
NC_000016.8:g.65122839A>T	NCBI36
NG_016862.1:g.23978T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.152T>A	ENSP00000299697.9:p.Leu51His
ENST00000417693.8:c.266T>A	ENSP00000407469.5:p.Leu89His
ENST00000451102.7:c.227T>A	ENSP00000414334.4:p.Leu76His
ENST00000527284.6:c.264T>A
ENST00000527800.6:c.29T>A	ENSP00000433770.1:p.Leu10His
ENST00000544898.6:c.320T>A MANE Select	ENSP00000440898.2:p.Leu107His
ENST00000567357.6:c.*178T>A	ENSP00000457959.2:n.*178T>A
ENST00000569718.6:c.227T>A	ENSP00000464313.2:p.Leu76His
ENST00000620035.5:c.245T>A	ENSP00000483833.2:p.Leu82His
ENST00000676538.1:c.33-13558T>A
ENST00000677379.1:c.35T>A	ENSP00000503672.1:p.Leu12His
ENST00000677420.1:c.29T>A	ENSP00000504648.1:p.Leu10His
ENST00000677497.1:n.207T>A
ENST00000677555.1:c.29T>A	ENSP00000503331.1:p.Leu10His
ENST00000677715.1:c.29T>A	ENSP00000502950.1:p.Leu10His
ENST00000677739.1:c.55-2368T>A	ENSP00000504644.1:n.55-2368T>A
ENST00000678015.1:c.29T>A	ENSP00000502959.1:p.Leu10His
ENST00000678297.1:c.29T>A	ENSP00000503472.1:p.Leu10His
ENST00000678314.1:c.29T>A	ENSP00000504438.1:p.Leu10His
ENST00000678746.1:c.210T>A	ENSP00000503227.1:n.210T>A
ENST00000679154.1:c.67T>A
ENST00000299697.11:c.320T>A	ENSP00000299697.8:p.Leu107His
ENST00000417693.7:c.392T>A	ENSP00000407469.4:p.Leu131His
ENST00000451102.6:c.446T>A	ENSP00000414334.3:p.Leu149His
ENST00000525974.5:c.29T>A	ENSP00000434594.1:p.Leu10His
ENST00000527284.5:c.227T>A	ENSP00000435312.1:p.Leu76His
ENST00000527800.5:c.29T>A	ENSP00000433770.1:p.Leu10His
ENST00000544898.5:c.320T>A	ENSP00000440898.2:p.Leu107His
ENST00000545043.6:c.245T>A	ENSP00000438143.2:p.Leu82His
ENST00000562484.2:c.29T>A	ENSP00000463326.1:p.Leu10His
ENST00000563369.6:c.29T>A	ENSP00000463560.1:p.Leu10His
ENST00000563478.5:c.29T>A	ENSP00000462341.1:p.Leu10His
ENST00000564917.5:c.320T>A	ENSP00000455187.1:p.Leu107His
ENST00000567357.5:c.*178T>A	ENSP00000457959.1:n.*178T>A
ENST00000569718.5:c.214T>A
ENST00000620035.4:c.266T>A	ENSP00000483833.1:p.Leu89His
NM_001172643.1:c.227T>A	NP_001166114.1:p.Leu76His
NM_001172644.1:c.245T>A	NP_001166115.1:p.Leu82His
NM_001172645.1:c.266T>A	NP_001166116.1:p.Leu89His
NM_001271934.1:c.173T>A	NP_001258863.1:p.Leu58His
NM_001271935.1:c.227T>A	NP_001258864.1:p.Leu76His
NM_001272050.1:c.29T>A	NP_001258979.1:p.Leu10His
NM_004614.4:c.320T>A	NP_004605.4:p.Leu107His
NR_073520.1:n.1599T>A
NM_001172644.2:c.245T>A	NP_001166115.1:p.Leu82His
NM_001271934.2:c.173T>A	NP_001258863.1:p.Leu58His
NM_001272050.2:c.29T>A	NP_001258979.1:p.Leu10His
NM_004614.5:c.320T>A MANE Select	NP_004605.4:p.Leu107His
NR_073520.2:n.1309T>A
NM_001172645.2:c.266T>A	NP_001166116.1:p.Leu89His