Canonical Allele Identifier: CA495902928

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547640A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513737A>C , CM000678.2:g.66513737A>C	GRCh38
NC_000016.9:g.66547640A>C , CM000678.1:g.66547640A>C	GRCh37
NC_000016.8:g.65105141A>C	NCBI36
NG_016862.1:g.41676T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.525T>G	ENSP00000299697.9:p.Pro175=
ENST00000417693.8:c.639T>G	ENSP00000407469.5:p.Pro213=
ENST00000451102.7:c.600T>G	ENSP00000414334.4:p.Pro200=
ENST00000527284.6:c.563-1671T>G
ENST00000527800.6:c.402T>G	ENSP00000433770.1:p.Pro134=
ENST00000544898.6:c.693T>G MANE Select	ENSP00000440898.2:p.Pro231=
ENST00000567357.6:c.*551T>G	ENSP00000457959.2:n.*551T>G
ENST00000569718.6:c.431T>G	ENSP00000464313.2:p.Leu144Arg
ENST00000620035.5:c.449T>G	ENSP00000483833.2:p.Leu150Arg
ENST00000676538.1:c.276T>G
ENST00000676904.1:c.164T>G
ENST00000677296.1:n.75T>G
ENST00000677379.1:c.334T>G	ENSP00000503672.1:n.334T>G
ENST00000677420.1:c.402T>G	ENSP00000504648.1:p.Pro134=
ENST00000677555.1:c.402T>G	ENSP00000503331.1:p.Pro134=
ENST00000677715.1:c.402T>G	ENSP00000502950.1:p.Pro134=
ENST00000677753.1:n.75T>G
ENST00000677961.1:n.105T>G
ENST00000678015.1:c.402T>G	ENSP00000502959.1:p.Pro134=
ENST00000678190.1:c.75T>G	ENSP00000503824.1:p.Pro25=
ENST00000678282.1:n.75T>G
ENST00000678297.1:c.402T>G	ENSP00000503472.1:p.Pro134=
ENST00000299697.11:c.693T>G	ENSP00000299697.8:p.Pro231=
ENST00000417693.7:c.765T>G	ENSP00000407469.4:p.Pro255=
ENST00000451102.6:c.819T>G	ENSP00000414334.3:p.Pro273=
ENST00000525974.5:c.402T>G	ENSP00000434594.1:p.Pro134=
ENST00000527284.5:c.600T>G	ENSP00000435312.1:p.Pro200=
ENST00000527800.5:c.402T>G	ENSP00000433770.1:p.Pro134=
ENST00000544898.5:c.693T>G	ENSP00000440898.2:p.Pro231=
ENST00000545043.6:c.618T>G	ENSP00000438143.2:p.Pro206=
ENST00000561527.5:n.252T>G
ENST00000561728.1:c.142T>G
ENST00000561905.2:c.47T>G
ENST00000562552.5:n.509T>G
ENST00000563099.5:n.220T>G
ENST00000563369.6:c.402T>G	ENSP00000463560.1:p.Pro134=
ENST00000564792.1:n.348T>G
ENST00000564917.5:c.744T>G	ENSP00000455187.1:p.Pro248=
ENST00000567357.5:c.*551T>G	ENSP00000457959.1:n.*551T>G
ENST00000569718.5:c.418T>G
ENST00000620035.4:c.639T>G	ENSP00000483833.1:p.Pro213=
NM_001172643.1:c.600T>G	NP_001166114.1:p.Pro200=
NM_001172644.1:c.618T>G	NP_001166115.1:p.Pro206=
NM_001172645.1:c.639T>G	NP_001166116.1:p.Pro213=
NM_001271934.1:c.546T>G	NP_001258863.1:p.Pro182=
NM_001271935.1:c.431T>G	NP_001258864.1:p.Leu144Arg
NM_001272050.1:c.402T>G	NP_001258979.1:p.Pro134=
NM_004614.4:c.693T>G	NP_004605.4:p.Pro231=
NR_073520.1:n.1972T>G
NM_001172644.2:c.618T>G	NP_001166115.1:p.Pro206=
NM_001271934.2:c.546T>G	NP_001258863.1:p.Pro182=
NM_001272050.2:c.402T>G	NP_001258979.1:p.Pro134=
NM_004614.5:c.693T>G MANE Select	NP_004605.4:p.Pro231=
NR_073520.2:n.1682T>G
NM_001172645.2:c.639T>G	NP_001166116.1:p.Pro213=