Canonical Allele Identifier: CA396187236

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547684C>A (hg19) ; chr16:g.66513781C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513781C>A , CM000678.2:g.66513781C>A	GRCh38
NC_000016.9:g.66547684C>A , CM000678.1:g.66547684C>A	GRCh37
NC_000016.8:g.65105185C>A	NCBI36
NG_016862.1:g.41632G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.481G>T	ENSP00000299697.9:p.Glu161Ter
ENST00000417693.8:c.595G>T	ENSP00000407469.5:p.Glu199Ter
ENST00000451102.7:c.556G>T	ENSP00000414334.4:p.Glu186Ter
ENST00000527284.6:c.563-1715G>T
ENST00000527800.6:c.358G>T	ENSP00000433770.1:p.Glu120Ter
ENST00000544898.6:c.649G>T MANE Select	ENSP00000440898.2:p.Glu217Ter
ENST00000567357.6:c.*507G>T	ENSP00000457959.2:n.*507G>T
ENST00000569718.6:c.387G>T	ENSP00000464313.2:p.Met129Ile
ENST00000620035.5:c.405G>T	ENSP00000483833.2:p.Met135Ile
ENST00000676538.1:c.232G>T
ENST00000676904.1:c.120G>T
ENST00000677296.1:n.31G>T
ENST00000677379.1:c.290G>T	ENSP00000503672.1:n.290G>T
ENST00000677420.1:c.358G>T	ENSP00000504648.1:p.Glu120Ter
ENST00000677555.1:c.358G>T	ENSP00000503331.1:p.Glu120Ter
ENST00000677715.1:c.358G>T	ENSP00000502950.1:p.Glu120Ter
ENST00000677753.1:n.31G>T
ENST00000677961.1:n.61G>T
ENST00000678015.1:c.358G>T	ENSP00000502959.1:p.Glu120Ter
ENST00000678190.1:c.31G>T	ENSP00000503824.1:p.Glu11Ter
ENST00000678282.1:n.31G>T
ENST00000678297.1:c.358G>T	ENSP00000503472.1:p.Glu120Ter
ENST00000299697.11:c.649G>T	ENSP00000299697.8:p.Glu217Ter
ENST00000417693.7:c.721G>T	ENSP00000407469.4:p.Glu241Ter
ENST00000451102.6:c.775G>T	ENSP00000414334.3:p.Glu259Ter
ENST00000525974.5:c.358G>T	ENSP00000434594.1:p.Glu120Ter
ENST00000527284.5:c.556G>T	ENSP00000435312.1:p.Glu186Ter
ENST00000527800.5:c.358G>T	ENSP00000433770.1:p.Glu120Ter
ENST00000544898.5:c.649G>T	ENSP00000440898.2:p.Glu217Ter
ENST00000545043.6:c.574G>T	ENSP00000438143.2:p.Glu192Ter
ENST00000561527.5:n.208G>T
ENST00000561728.1:c.98G>T
ENST00000561905.2:c.3G>T
ENST00000562552.5:n.465G>T
ENST00000563099.5:n.176G>T
ENST00000563369.6:c.358G>T	ENSP00000463560.1:p.Glu120Ter
ENST00000563478.5:c.358G>T	ENSP00000462341.1:p.Glu120Ter
ENST00000564792.1:n.304G>T
ENST00000564917.5:c.700G>T	ENSP00000455187.1:p.Glu234Ter
ENST00000567357.5:c.*507G>T	ENSP00000457959.1:n.*507G>T
ENST00000569718.5:c.374G>T
ENST00000620035.4:c.595G>T	ENSP00000483833.1:p.Glu199Ter
NM_001172643.1:c.556G>T	NP_001166114.1:p.Glu186Ter
NM_001172644.1:c.574G>T	NP_001166115.1:p.Glu192Ter
NM_001172645.1:c.595G>T	NP_001166116.1:p.Glu199Ter
NM_001271934.1:c.502G>T	NP_001258863.1:p.Glu168Ter
NM_001271935.1:c.387G>T	NP_001258864.1:p.Met129Ile
NM_001272050.1:c.358G>T	NP_001258979.1:p.Glu120Ter
NM_004614.4:c.649G>T	NP_004605.4:p.Glu217Ter
NR_073520.1:n.1928G>T
NM_001172644.2:c.574G>T	NP_001166115.1:p.Glu192Ter
NM_001271934.2:c.502G>T	NP_001258863.1:p.Glu168Ter
NM_001272050.2:c.358G>T	NP_001258979.1:p.Glu120Ter
NM_004614.5:c.649G>T MANE Select	NP_004605.4:p.Glu217Ter
NR_073520.2:n.1638G>T
NM_001172645.2:c.595G>T	NP_001166116.1:p.Glu199Ter