Canonical Allele Identifier: CA495902941

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547646T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513743T>G , CM000678.2:g.66513743T>G	GRCh38
NC_000016.9:g.66547646T>G , CM000678.1:g.66547646T>G	GRCh37
NC_000016.8:g.65105147T>G	NCBI36
NG_016862.1:g.41670A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.519A>C	ENSP00000299697.9:p.Ala173=
ENST00000417693.8:c.633A>C	ENSP00000407469.5:p.Ala211=
ENST00000451102.7:c.594A>C	ENSP00000414334.4:p.Ala198=
ENST00000527284.6:c.563-1677A>C
ENST00000527800.6:c.396A>C	ENSP00000433770.1:p.Ala132=
ENST00000544898.6:c.687A>C MANE Select	ENSP00000440898.2:p.Ala229=
ENST00000567357.6:c.*545A>C	ENSP00000457959.2:n.*545A>C
ENST00000569718.6:c.425A>C	ENSP00000464313.2:p.Gln142Pro
ENST00000620035.5:c.443A>C	ENSP00000483833.2:p.Gln148Pro
ENST00000676538.1:c.270A>C
ENST00000676904.1:c.158A>C
ENST00000677296.1:n.69A>C
ENST00000677379.1:c.328A>C	ENSP00000503672.1:n.328A>C
ENST00000677420.1:c.396A>C	ENSP00000504648.1:p.Ala132=
ENST00000677555.1:c.396A>C	ENSP00000503331.1:p.Ala132=
ENST00000677715.1:c.396A>C	ENSP00000502950.1:p.Ala132=
ENST00000677753.1:n.69A>C
ENST00000677961.1:n.99A>C
ENST00000678015.1:c.396A>C	ENSP00000502959.1:p.Ala132=
ENST00000678190.1:c.69A>C	ENSP00000503824.1:p.Ala23=
ENST00000678282.1:n.69A>C
ENST00000678297.1:c.396A>C	ENSP00000503472.1:p.Ala132=
ENST00000299697.11:c.687A>C	ENSP00000299697.8:p.Ala229=
ENST00000417693.7:c.759A>C	ENSP00000407469.4:p.Ala253=
ENST00000451102.6:c.813A>C	ENSP00000414334.3:p.Ala271=
ENST00000525974.5:c.396A>C	ENSP00000434594.1:p.Ala132=
ENST00000527284.5:c.594A>C	ENSP00000435312.1:p.Ala198=
ENST00000527800.5:c.396A>C	ENSP00000433770.1:p.Ala132=
ENST00000544898.5:c.687A>C	ENSP00000440898.2:p.Ala229=
ENST00000545043.6:c.612A>C	ENSP00000438143.2:p.Ala204=
ENST00000561527.5:n.246A>C
ENST00000561728.1:c.136A>C
ENST00000561905.2:c.41A>C
ENST00000562552.5:n.503A>C
ENST00000563099.5:n.214A>C
ENST00000563369.6:c.396A>C	ENSP00000463560.1:p.Ala132=
ENST00000564792.1:n.342A>C
ENST00000564917.5:c.738A>C	ENSP00000455187.1:p.Ala246=
ENST00000567357.5:c.*545A>C	ENSP00000457959.1:n.*545A>C
ENST00000569718.5:c.412A>C
ENST00000620035.4:c.633A>C	ENSP00000483833.1:p.Ala211=
NM_001172643.1:c.594A>C	NP_001166114.1:p.Ala198=
NM_001172644.1:c.612A>C	NP_001166115.1:p.Ala204=
NM_001172645.1:c.633A>C	NP_001166116.1:p.Ala211=
NM_001271934.1:c.540A>C	NP_001258863.1:p.Ala180=
NM_001271935.1:c.425A>C	NP_001258864.1:p.Gln142Pro
NM_001272050.1:c.396A>C	NP_001258979.1:p.Ala132=
NM_004614.4:c.687A>C	NP_004605.4:p.Ala229=
NR_073520.1:n.1966A>C
NM_001172644.2:c.612A>C	NP_001166115.1:p.Ala204=
NM_001271934.2:c.540A>C	NP_001258863.1:p.Ala180=
NM_001272050.2:c.396A>C	NP_001258979.1:p.Ala132=
NM_004614.5:c.687A>C MANE Select	NP_004605.4:p.Ala229=
NR_073520.2:n.1676A>C
NM_001172645.2:c.633A>C	NP_001166116.1:p.Ala211=