Canonical Allele Identifier: CA495902923

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547636G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513733G>A , CM000678.2:g.66513733G>A	GRCh38
NC_000016.9:g.66547636G>A , CM000678.1:g.66547636G>A	GRCh37
NC_000016.8:g.65105137G>A	NCBI36
NG_016862.1:g.41680C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.529C>T	ENSP00000299697.9:p.Leu177=
ENST00000417693.8:c.643C>T	ENSP00000407469.5:p.Leu215=
ENST00000451102.7:c.604C>T	ENSP00000414334.4:p.Leu202=
ENST00000527284.6:c.563-1667C>T
ENST00000527800.6:c.406C>T	ENSP00000433770.1:p.Leu136=
ENST00000544898.6:c.697C>T MANE Select	ENSP00000440898.2:p.Leu233=
ENST00000567357.6:c.*555C>T	ENSP00000457959.2:n.*555C>T
ENST00000569718.6:c.435C>T	ENSP00000464313.2:p.Phe145=
ENST00000620035.5:c.453C>T	ENSP00000483833.2:p.Phe151=
ENST00000676538.1:c.280C>T
ENST00000676904.1:c.168C>T
ENST00000677296.1:n.79C>T
ENST00000677379.1:c.338C>T	ENSP00000503672.1:n.338C>T
ENST00000677420.1:c.406C>T	ENSP00000504648.1:p.Leu136=
ENST00000677555.1:c.406C>T	ENSP00000503331.1:p.Leu136=
ENST00000677715.1:c.406C>T	ENSP00000502950.1:p.Leu136=
ENST00000677753.1:n.79C>T
ENST00000677961.1:n.109C>T
ENST00000678015.1:c.406C>T	ENSP00000502959.1:p.Leu136=
ENST00000678190.1:c.79C>T	ENSP00000503824.1:p.Leu27=
ENST00000678282.1:n.79C>T
ENST00000678297.1:c.406C>T	ENSP00000503472.1:p.Leu136=
ENST00000299697.11:c.697C>T	ENSP00000299697.8:p.Leu233=
ENST00000417693.7:c.769C>T	ENSP00000407469.4:p.Leu257=
ENST00000451102.6:c.823C>T	ENSP00000414334.3:p.Leu275=
ENST00000525974.5:c.406C>T	ENSP00000434594.1:p.Leu136=
ENST00000527284.5:c.604C>T	ENSP00000435312.1:p.Leu202=
ENST00000527800.5:c.406C>T	ENSP00000433770.1:p.Leu136=
ENST00000544898.5:c.697C>T	ENSP00000440898.2:p.Leu233=
ENST00000545043.6:c.622C>T	ENSP00000438143.2:p.Leu208=
ENST00000561527.5:n.256C>T
ENST00000561728.1:c.146C>T
ENST00000561905.2:c.51C>T
ENST00000562552.5:n.513C>T
ENST00000563099.5:n.224C>T
ENST00000563369.6:c.406C>T	ENSP00000463560.1:p.Leu136=
ENST00000564792.1:n.352C>T
ENST00000564917.5:c.748C>T	ENSP00000455187.1:p.Leu250=
ENST00000567357.5:c.*555C>T	ENSP00000457959.1:n.*555C>T
ENST00000569718.5:c.422C>T
ENST00000620035.4:c.643C>T	ENSP00000483833.1:p.Leu215=
NM_001172643.1:c.604C>T	NP_001166114.1:p.Leu202=
NM_001172644.1:c.622C>T	NP_001166115.1:p.Leu208=
NM_001172645.1:c.643C>T	NP_001166116.1:p.Leu215=
NM_001271934.1:c.550C>T	NP_001258863.1:p.Leu184=
NM_001271935.1:c.435C>T	NP_001258864.1:p.Phe145=
NM_001272050.1:c.406C>T	NP_001258979.1:p.Leu136=
NM_004614.4:c.697C>T	NP_004605.4:p.Leu233=
NR_073520.1:n.1976C>T
NM_001172644.2:c.622C>T	NP_001166115.1:p.Leu208=
NM_001271934.2:c.550C>T	NP_001258863.1:p.Leu184=
NM_001272050.2:c.406C>T	NP_001258979.1:p.Leu136=
NM_004614.5:c.697C>T MANE Select	NP_004605.4:p.Leu233=
NR_073520.2:n.1686C>T
NM_001172645.2:c.643C>T	NP_001166116.1:p.Leu215=