Canonical Allele Identifier: CA396187124

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547662C>G (hg19) ; chr16:g.66513759C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513759C>G , CM000678.2:g.66513759C>G	GRCh38
NC_000016.9:g.66547662C>G , CM000678.1:g.66547662C>G	GRCh37
NC_000016.8:g.65105163C>G	NCBI36
NG_016862.1:g.41654G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.503G>C	ENSP00000299697.9:p.Ser168Thr
ENST00000417693.8:c.617G>C	ENSP00000407469.5:p.Ser206Thr
ENST00000451102.7:c.578G>C	ENSP00000414334.4:p.Ser193Thr
ENST00000527284.6:c.563-1693G>C
ENST00000527800.6:c.380G>C	ENSP00000433770.1:p.Ser127Thr
ENST00000544898.6:c.671G>C MANE Select	ENSP00000440898.2:p.Ser224Thr
ENST00000567357.6:c.*529G>C	ENSP00000457959.2:n.*529G>C
ENST00000569718.6:c.409G>C	ENSP00000464313.2:p.Ala137Pro
ENST00000620035.5:c.427G>C	ENSP00000483833.2:p.Ala143Pro
ENST00000676538.1:c.254G>C
ENST00000676904.1:c.142G>C
ENST00000677296.1:n.53G>C
ENST00000677379.1:c.312G>C	ENSP00000503672.1:n.312G>C
ENST00000677420.1:c.380G>C	ENSP00000504648.1:p.Ser127Thr
ENST00000677555.1:c.380G>C	ENSP00000503331.1:p.Ser127Thr
ENST00000677715.1:c.380G>C	ENSP00000502950.1:p.Ser127Thr
ENST00000677753.1:n.53G>C
ENST00000677961.1:n.83G>C
ENST00000678015.1:c.380G>C	ENSP00000502959.1:p.Ser127Thr
ENST00000678190.1:c.53G>C	ENSP00000503824.1:p.Ser18Thr
ENST00000678282.1:n.53G>C
ENST00000678297.1:c.380G>C	ENSP00000503472.1:p.Ser127Thr
ENST00000299697.11:c.671G>C	ENSP00000299697.8:p.Ser224Thr
ENST00000417693.7:c.743G>C	ENSP00000407469.4:p.Ser248Thr
ENST00000451102.6:c.797G>C	ENSP00000414334.3:p.Ser266Thr
ENST00000525974.5:c.380G>C	ENSP00000434594.1:p.Ser127Thr
ENST00000527284.5:c.578G>C	ENSP00000435312.1:p.Ser193Thr
ENST00000527800.5:c.380G>C	ENSP00000433770.1:p.Ser127Thr
ENST00000544898.5:c.671G>C	ENSP00000440898.2:p.Ser224Thr
ENST00000545043.6:c.596G>C	ENSP00000438143.2:p.Ser199Thr
ENST00000561527.5:n.230G>C
ENST00000561728.1:c.120G>C
ENST00000561905.2:c.25G>C
ENST00000562552.5:n.487G>C
ENST00000563099.5:n.198G>C
ENST00000563369.6:c.380G>C	ENSP00000463560.1:p.Ser127Thr
ENST00000563478.5:c.380G>C	ENSP00000462341.1:p.Ser127Thr
ENST00000564792.1:n.326G>C
ENST00000564917.5:c.722G>C	ENSP00000455187.1:p.Ser241Thr
ENST00000567357.5:c.*529G>C	ENSP00000457959.1:n.*529G>C
ENST00000569718.5:c.396G>C
ENST00000620035.4:c.617G>C	ENSP00000483833.1:p.Ser206Thr
NM_001172643.1:c.578G>C	NP_001166114.1:p.Ser193Thr
NM_001172644.1:c.596G>C	NP_001166115.1:p.Ser199Thr
NM_001172645.1:c.617G>C	NP_001166116.1:p.Ser206Thr
NM_001271934.1:c.524G>C	NP_001258863.1:p.Ser175Thr
NM_001271935.1:c.409G>C	NP_001258864.1:p.Ala137Pro
NM_001272050.1:c.380G>C	NP_001258979.1:p.Ser127Thr
NM_004614.4:c.671G>C	NP_004605.4:p.Ser224Thr
NR_073520.1:n.1950G>C
NM_001172644.2:c.596G>C	NP_001166115.1:p.Ser199Thr
NM_001271934.2:c.524G>C	NP_001258863.1:p.Ser175Thr
NM_001272050.2:c.380G>C	NP_001258979.1:p.Ser127Thr
NM_004614.5:c.671G>C MANE Select	NP_004605.4:p.Ser224Thr
NR_073520.2:n.1660G>C
NM_001172645.2:c.617G>C	NP_001166116.1:p.Ser206Thr