Canonical Allele Identifier: CA495902949

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547652G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513749G>C , CM000678.2:g.66513749G>C	GRCh38
NC_000016.9:g.66547652G>C , CM000678.1:g.66547652G>C	GRCh37
NC_000016.8:g.65105153G>C	NCBI36
NG_016862.1:g.41664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.513C>G	ENSP00000299697.9:p.Pro171=
ENST00000417693.8:c.627C>G	ENSP00000407469.5:p.Pro209=
ENST00000451102.7:c.588C>G	ENSP00000414334.4:p.Pro196=
ENST00000527284.6:c.563-1683C>G
ENST00000527800.6:c.390C>G	ENSP00000433770.1:p.Pro130=
ENST00000544898.6:c.681C>G MANE Select	ENSP00000440898.2:p.Pro227=
ENST00000567357.6:c.*539C>G	ENSP00000457959.2:n.*539C>G
ENST00000569718.6:c.419C>G	ENSP00000464313.2:p.Pro140Arg
ENST00000620035.5:c.437C>G	ENSP00000483833.2:p.Pro146Arg
ENST00000676538.1:c.264C>G
ENST00000676904.1:c.152C>G
ENST00000677296.1:n.63C>G
ENST00000677379.1:c.322C>G	ENSP00000503672.1:n.322C>G
ENST00000677420.1:c.390C>G	ENSP00000504648.1:p.Pro130=
ENST00000677555.1:c.390C>G	ENSP00000503331.1:p.Pro130=
ENST00000677715.1:c.390C>G	ENSP00000502950.1:p.Pro130=
ENST00000677753.1:n.63C>G
ENST00000677961.1:n.93C>G
ENST00000678015.1:c.390C>G	ENSP00000502959.1:p.Pro130=
ENST00000678190.1:c.63C>G	ENSP00000503824.1:p.Pro21=
ENST00000678282.1:n.63C>G
ENST00000678297.1:c.390C>G	ENSP00000503472.1:p.Pro130=
ENST00000299697.11:c.681C>G	ENSP00000299697.8:p.Pro227=
ENST00000417693.7:c.753C>G	ENSP00000407469.4:p.Pro251=
ENST00000451102.6:c.807C>G	ENSP00000414334.3:p.Pro269=
ENST00000525974.5:c.390C>G	ENSP00000434594.1:p.Pro130=
ENST00000527284.5:c.588C>G	ENSP00000435312.1:p.Pro196=
ENST00000527800.5:c.390C>G	ENSP00000433770.1:p.Pro130=
ENST00000544898.5:c.681C>G	ENSP00000440898.2:p.Pro227=
ENST00000545043.6:c.606C>G	ENSP00000438143.2:p.Pro202=
ENST00000561527.5:n.240C>G
ENST00000561728.1:c.130C>G
ENST00000561905.2:c.35C>G
ENST00000562552.5:n.497C>G
ENST00000563099.5:n.208C>G
ENST00000563369.6:c.390C>G	ENSP00000463560.1:p.Pro130=
ENST00000563478.5:c.390C>G	ENSP00000462341.1:p.Pro130=
ENST00000564792.1:n.336C>G
ENST00000564917.5:c.732C>G	ENSP00000455187.1:p.Pro244=
ENST00000567357.5:c.*539C>G	ENSP00000457959.1:n.*539C>G
ENST00000569718.5:c.406C>G
ENST00000620035.4:c.627C>G	ENSP00000483833.1:p.Pro209=
NM_001172643.1:c.588C>G	NP_001166114.1:p.Pro196=
NM_001172644.1:c.606C>G	NP_001166115.1:p.Pro202=
NM_001172645.1:c.627C>G	NP_001166116.1:p.Pro209=
NM_001271934.1:c.534C>G	NP_001258863.1:p.Pro178=
NM_001271935.1:c.419C>G	NP_001258864.1:p.Pro140Arg
NM_001272050.1:c.390C>G	NP_001258979.1:p.Pro130=
NM_004614.4:c.681C>G	NP_004605.4:p.Pro227=
NR_073520.1:n.1960C>G
NM_001172644.2:c.606C>G	NP_001166115.1:p.Pro202=
NM_001271934.2:c.534C>G	NP_001258863.1:p.Pro178=
NM_001272050.2:c.390C>G	NP_001258979.1:p.Pro130=
NM_004614.5:c.681C>G MANE Select	NP_004605.4:p.Pro227=
NR_073520.2:n.1670C>G
NM_001172645.2:c.627C>G	NP_001166116.1:p.Pro209=