Canonical Allele Identifier: CA396187062

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547647G>T (hg19) ; chr16:g.66513744G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513744G>T , CM000678.2:g.66513744G>T	GRCh38
NC_000016.9:g.66547647G>T , CM000678.1:g.66547647G>T	GRCh37
NC_000016.8:g.65105148G>T	NCBI36
NG_016862.1:g.41669C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.518C>A	ENSP00000299697.9:p.Ala173Glu
ENST00000417693.8:c.632C>A	ENSP00000407469.5:p.Ala211Glu
ENST00000451102.7:c.593C>A	ENSP00000414334.4:p.Ala198Glu
ENST00000527284.6:c.563-1678C>A
ENST00000527800.6:c.395C>A	ENSP00000433770.1:p.Ala132Glu
ENST00000544898.6:c.686C>A MANE Select	ENSP00000440898.2:p.Ala229Glu
ENST00000567357.6:c.*544C>A	ENSP00000457959.2:n.*544C>A
ENST00000569718.6:c.424C>A	ENSP00000464313.2:p.Gln142Lys
ENST00000620035.5:c.442C>A	ENSP00000483833.2:p.Gln148Lys
ENST00000676538.1:c.269C>A
ENST00000676904.1:c.157C>A
ENST00000677296.1:n.68C>A
ENST00000677379.1:c.327C>A	ENSP00000503672.1:n.327C>A
ENST00000677420.1:c.395C>A	ENSP00000504648.1:p.Ala132Glu
ENST00000677555.1:c.395C>A	ENSP00000503331.1:p.Ala132Glu
ENST00000677715.1:c.395C>A	ENSP00000502950.1:p.Ala132Glu
ENST00000677753.1:n.68C>A
ENST00000677961.1:n.98C>A
ENST00000678015.1:c.395C>A	ENSP00000502959.1:p.Ala132Glu
ENST00000678190.1:c.68C>A	ENSP00000503824.1:p.Ala23Glu
ENST00000678282.1:n.68C>A
ENST00000678297.1:c.395C>A	ENSP00000503472.1:p.Ala132Glu
ENST00000299697.11:c.686C>A	ENSP00000299697.8:p.Ala229Glu
ENST00000417693.7:c.758C>A	ENSP00000407469.4:p.Ala253Glu
ENST00000451102.6:c.812C>A	ENSP00000414334.3:p.Ala271Glu
ENST00000525974.5:c.395C>A	ENSP00000434594.1:p.Ala132Glu
ENST00000527284.5:c.593C>A	ENSP00000435312.1:p.Ala198Glu
ENST00000527800.5:c.395C>A	ENSP00000433770.1:p.Ala132Glu
ENST00000544898.5:c.686C>A	ENSP00000440898.2:p.Ala229Glu
ENST00000545043.6:c.611C>A	ENSP00000438143.2:p.Ala204Glu
ENST00000561527.5:n.245C>A
ENST00000561728.1:c.135C>A
ENST00000561905.2:c.40C>A
ENST00000562552.5:n.502C>A
ENST00000563099.5:n.213C>A
ENST00000563369.6:c.395C>A	ENSP00000463560.1:p.Ala132Glu
ENST00000564792.1:n.341C>A
ENST00000564917.5:c.737C>A	ENSP00000455187.1:p.Ala246Glu
ENST00000567357.5:c.*544C>A	ENSP00000457959.1:n.*544C>A
ENST00000569718.5:c.411C>A
ENST00000620035.4:c.632C>A	ENSP00000483833.1:p.Ala211Glu
NM_001172643.1:c.593C>A	NP_001166114.1:p.Ala198Glu
NM_001172644.1:c.611C>A	NP_001166115.1:p.Ala204Glu
NM_001172645.1:c.632C>A	NP_001166116.1:p.Ala211Glu
NM_001271934.1:c.539C>A	NP_001258863.1:p.Ala180Glu
NM_001271935.1:c.424C>A	NP_001258864.1:p.Gln142Lys
NM_001272050.1:c.395C>A	NP_001258979.1:p.Ala132Glu
NM_004614.4:c.686C>A	NP_004605.4:p.Ala229Glu
NR_073520.1:n.1965C>A
NM_001172644.2:c.611C>A	NP_001166115.1:p.Ala204Glu
NM_001271934.2:c.539C>A	NP_001258863.1:p.Ala180Glu
NM_001272050.2:c.395C>A	NP_001258979.1:p.Ala132Glu
NM_004614.5:c.686C>A MANE Select	NP_004605.4:p.Ala229Glu
NR_073520.2:n.1675C>A
NM_001172645.2:c.632C>A	NP_001166116.1:p.Ala211Glu