Canonical Allele Identifier: CA396187219

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547681C>G (hg19) ; chr16:g.66513778C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513778C>G , CM000678.2:g.66513778C>G	GRCh38
NC_000016.9:g.66547681C>G , CM000678.1:g.66547681C>G	GRCh37
NC_000016.8:g.65105182C>G	NCBI36
NG_016862.1:g.41635G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.484G>C	ENSP00000299697.9:p.Glu162Gln
ENST00000417693.8:c.598G>C	ENSP00000407469.5:p.Glu200Gln
ENST00000451102.7:c.559G>C	ENSP00000414334.4:p.Glu187Gln
ENST00000527284.6:c.563-1712G>C
ENST00000527800.6:c.361G>C	ENSP00000433770.1:p.Glu121Gln
ENST00000544898.6:c.652G>C MANE Select	ENSP00000440898.2:p.Glu218Gln
ENST00000567357.6:c.*510G>C	ENSP00000457959.2:n.*510G>C
ENST00000569718.6:c.390G>C	ENSP00000464313.2:p.Arg130Ser
ENST00000620035.5:c.408G>C	ENSP00000483833.2:p.Arg136Ser
ENST00000676538.1:c.235G>C
ENST00000676904.1:c.123G>C
ENST00000677296.1:n.34G>C
ENST00000677379.1:c.293G>C	ENSP00000503672.1:n.293G>C
ENST00000677420.1:c.361G>C	ENSP00000504648.1:p.Glu121Gln
ENST00000677555.1:c.361G>C	ENSP00000503331.1:p.Glu121Gln
ENST00000677715.1:c.361G>C	ENSP00000502950.1:p.Glu121Gln
ENST00000677753.1:n.34G>C
ENST00000677961.1:n.64G>C
ENST00000678015.1:c.361G>C	ENSP00000502959.1:p.Glu121Gln
ENST00000678190.1:c.34G>C	ENSP00000503824.1:p.Glu12Gln
ENST00000678282.1:n.34G>C
ENST00000678297.1:c.361G>C	ENSP00000503472.1:p.Glu121Gln
ENST00000299697.11:c.652G>C	ENSP00000299697.8:p.Glu218Gln
ENST00000417693.7:c.724G>C	ENSP00000407469.4:p.Glu242Gln
ENST00000451102.6:c.778G>C	ENSP00000414334.3:p.Glu260Gln
ENST00000525974.5:c.361G>C	ENSP00000434594.1:p.Glu121Gln
ENST00000527284.5:c.559G>C	ENSP00000435312.1:p.Glu187Gln
ENST00000527800.5:c.361G>C	ENSP00000433770.1:p.Glu121Gln
ENST00000544898.5:c.652G>C	ENSP00000440898.2:p.Glu218Gln
ENST00000545043.6:c.577G>C	ENSP00000438143.2:p.Glu193Gln
ENST00000561527.5:n.211G>C
ENST00000561728.1:c.101G>C
ENST00000561905.2:c.6G>C
ENST00000562552.5:n.468G>C
ENST00000563099.5:n.179G>C
ENST00000563369.6:c.361G>C	ENSP00000463560.1:p.Glu121Gln
ENST00000563478.5:c.361G>C	ENSP00000462341.1:p.Glu121Gln
ENST00000564792.1:n.307G>C
ENST00000564917.5:c.703G>C	ENSP00000455187.1:p.Glu235Gln
ENST00000567357.5:c.*510G>C	ENSP00000457959.1:n.*510G>C
ENST00000569718.5:c.377G>C
ENST00000620035.4:c.598G>C	ENSP00000483833.1:p.Glu200Gln
NM_001172643.1:c.559G>C	NP_001166114.1:p.Glu187Gln
NM_001172644.1:c.577G>C	NP_001166115.1:p.Glu193Gln
NM_001172645.1:c.598G>C	NP_001166116.1:p.Glu200Gln
NM_001271934.1:c.505G>C	NP_001258863.1:p.Glu169Gln
NM_001271935.1:c.390G>C	NP_001258864.1:p.Arg130Ser
NM_001272050.1:c.361G>C	NP_001258979.1:p.Glu121Gln
NM_004614.4:c.652G>C	NP_004605.4:p.Glu218Gln
NR_073520.1:n.1931G>C
NM_001172644.2:c.577G>C	NP_001166115.1:p.Glu193Gln
NM_001271934.2:c.505G>C	NP_001258863.1:p.Glu169Gln
NM_001272050.2:c.361G>C	NP_001258979.1:p.Glu121Gln
NM_004614.5:c.652G>C MANE Select	NP_004605.4:p.Glu218Gln
NR_073520.2:n.1641G>C
NM_001172645.2:c.598G>C	NP_001166116.1:p.Glu200Gln