Canonical Allele Identifier: CA396190633

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66565339G>C (hg19) ; chr16:g.66531436G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531436G>C , CM000678.2:g.66531436G>C	GRCh38
NC_000016.9:g.66565339G>C , CM000678.1:g.66565339G>C	GRCh37
NC_000016.8:g.65122840G>C	NCBI36
NG_016862.1:g.23977C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.151C>G	ENSP00000299697.9:p.Leu51Val
ENST00000417693.8:c.265C>G	ENSP00000407469.5:p.Leu89Val
ENST00000451102.7:c.226C>G	ENSP00000414334.4:p.Leu76Val
ENST00000527284.6:c.263C>G
ENST00000527800.6:c.28C>G	ENSP00000433770.1:p.Leu10Val
ENST00000544898.6:c.319C>G MANE Select	ENSP00000440898.2:p.Leu107Val
ENST00000567357.6:c.*177C>G	ENSP00000457959.2:n.*177C>G
ENST00000569718.6:c.226C>G	ENSP00000464313.2:p.Leu76Val
ENST00000620035.5:c.244C>G	ENSP00000483833.2:p.Leu82Val
ENST00000676538.1:c.33-13559C>G
ENST00000677379.1:c.34C>G	ENSP00000503672.1:p.Leu12Val
ENST00000677420.1:c.28C>G	ENSP00000504648.1:p.Leu10Val
ENST00000677497.1:n.206C>G
ENST00000677555.1:c.28C>G	ENSP00000503331.1:p.Leu10Val
ENST00000677715.1:c.28C>G	ENSP00000502950.1:p.Leu10Val
ENST00000677739.1:c.55-2369C>G	ENSP00000504644.1:n.55-2369C>G
ENST00000678015.1:c.28C>G	ENSP00000502959.1:p.Leu10Val
ENST00000678297.1:c.28C>G	ENSP00000503472.1:p.Leu10Val
ENST00000678314.1:c.28C>G	ENSP00000504438.1:p.Leu10Val
ENST00000678746.1:c.209C>G	ENSP00000503227.1:n.209C>G
ENST00000679154.1:c.66C>G
ENST00000299697.11:c.319C>G	ENSP00000299697.8:p.Leu107Val
ENST00000417693.7:c.391C>G	ENSP00000407469.4:p.Leu131Val
ENST00000451102.6:c.445C>G	ENSP00000414334.3:p.Leu149Val
ENST00000525974.5:c.28C>G	ENSP00000434594.1:p.Leu10Val
ENST00000527284.5:c.226C>G	ENSP00000435312.1:p.Leu76Val
ENST00000527800.5:c.28C>G	ENSP00000433770.1:p.Leu10Val
ENST00000544898.5:c.319C>G	ENSP00000440898.2:p.Leu107Val
ENST00000545043.6:c.244C>G	ENSP00000438143.2:p.Leu82Val
ENST00000562484.2:c.28C>G	ENSP00000463326.1:p.Leu10Val
ENST00000563369.6:c.28C>G	ENSP00000463560.1:p.Leu10Val
ENST00000563478.5:c.28C>G	ENSP00000462341.1:p.Leu10Val
ENST00000564917.5:c.319C>G	ENSP00000455187.1:p.Leu107Val
ENST00000567357.5:c.*177C>G	ENSP00000457959.1:n.*177C>G
ENST00000569718.5:c.213C>G
ENST00000620035.4:c.265C>G	ENSP00000483833.1:p.Leu89Val
NM_001172643.1:c.226C>G	NP_001166114.1:p.Leu76Val
NM_001172644.1:c.244C>G	NP_001166115.1:p.Leu82Val
NM_001172645.1:c.265C>G	NP_001166116.1:p.Leu89Val
NM_001271934.1:c.172C>G	NP_001258863.1:p.Leu58Val
NM_001271935.1:c.226C>G	NP_001258864.1:p.Leu76Val
NM_001272050.1:c.28C>G	NP_001258979.1:p.Leu10Val
NM_004614.4:c.319C>G	NP_004605.4:p.Leu107Val
NR_073520.1:n.1598C>G
NM_001172644.2:c.244C>G	NP_001166115.1:p.Leu82Val
NM_001271934.2:c.172C>G	NP_001258863.1:p.Leu58Val
NM_001272050.2:c.28C>G	NP_001258979.1:p.Leu10Val
NM_004614.5:c.319C>G MANE Select	NP_004605.4:p.Leu107Val
NR_073520.2:n.1308C>G
NM_001172645.2:c.265C>G	NP_001166116.1:p.Leu89Val