Canonical Allele Identifier: CA495906105

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66565340A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531437A>G , CM000678.2:g.66531437A>G	GRCh38
NC_000016.9:g.66565340A>G , CM000678.1:g.66565340A>G	GRCh37
NC_000016.8:g.65122841A>G	NCBI36
NG_016862.1:g.23976T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.150T>C	ENSP00000299697.9:p.Gly50=
ENST00000417693.8:c.264T>C	ENSP00000407469.5:p.Gly88=
ENST00000451102.7:c.225T>C	ENSP00000414334.4:p.Gly75=
ENST00000527284.6:c.262T>C
ENST00000527800.6:c.27T>C	ENSP00000433770.1:p.Gly9=
ENST00000544898.6:c.318T>C MANE Select	ENSP00000440898.2:p.Gly106=
ENST00000567357.6:c.*176T>C	ENSP00000457959.2:n.*176T>C
ENST00000569718.6:c.225T>C	ENSP00000464313.2:p.Gly75=
ENST00000620035.5:c.243T>C	ENSP00000483833.2:p.Gly81=
ENST00000676538.1:c.33-13560T>C
ENST00000677379.1:c.33T>C	ENSP00000503672.1:p.Gly11=
ENST00000677420.1:c.27T>C	ENSP00000504648.1:p.Gly9=
ENST00000677497.1:n.205T>C
ENST00000677555.1:c.27T>C	ENSP00000503331.1:p.Gly9=
ENST00000677715.1:c.27T>C	ENSP00000502950.1:p.Gly9=
ENST00000677739.1:c.55-2370T>C	ENSP00000504644.1:n.55-2370T>C
ENST00000678015.1:c.27T>C	ENSP00000502959.1:p.Gly9=
ENST00000678297.1:c.27T>C	ENSP00000503472.1:p.Gly9=
ENST00000678314.1:c.27T>C	ENSP00000504438.1:p.Gly9=
ENST00000678746.1:c.208T>C	ENSP00000503227.1:n.208T>C
ENST00000679154.1:c.65T>C
ENST00000299697.11:c.318T>C	ENSP00000299697.8:p.Gly106=
ENST00000417693.7:c.390T>C	ENSP00000407469.4:p.Gly130=
ENST00000451102.6:c.444T>C	ENSP00000414334.3:p.Gly148=
ENST00000525974.5:c.27T>C	ENSP00000434594.1:p.Gly9=
ENST00000527284.5:c.225T>C	ENSP00000435312.1:p.Gly75=
ENST00000527800.5:c.27T>C	ENSP00000433770.1:p.Gly9=
ENST00000544898.5:c.318T>C	ENSP00000440898.2:p.Gly106=
ENST00000545043.6:c.243T>C	ENSP00000438143.2:p.Gly81=
ENST00000562484.2:c.27T>C	ENSP00000463326.1:p.Gly9=
ENST00000563369.6:c.27T>C	ENSP00000463560.1:p.Gly9=
ENST00000563478.5:c.27T>C	ENSP00000462341.1:p.Gly9=
ENST00000564917.5:c.318T>C	ENSP00000455187.1:p.Gly106=
ENST00000567357.5:c.*176T>C	ENSP00000457959.1:n.*176T>C
ENST00000569718.5:c.212T>C
ENST00000620035.4:c.264T>C	ENSP00000483833.1:p.Gly88=
NM_001172643.1:c.225T>C	NP_001166114.1:p.Gly75=
NM_001172644.1:c.243T>C	NP_001166115.1:p.Gly81=
NM_001172645.1:c.264T>C	NP_001166116.1:p.Gly88=
NM_001271934.1:c.171T>C	NP_001258863.1:p.Gly57=
NM_001271935.1:c.225T>C	NP_001258864.1:p.Gly75=
NM_001272050.1:c.27T>C	NP_001258979.1:p.Gly9=
NM_004614.4:c.318T>C	NP_004605.4:p.Gly106=
NR_073520.1:n.1597T>C
NM_001172644.2:c.243T>C	NP_001166115.1:p.Gly81=
NM_001271934.2:c.171T>C	NP_001258863.1:p.Gly57=
NM_001272050.2:c.27T>C	NP_001258979.1:p.Gly9=
NM_004614.5:c.318T>C MANE Select	NP_004605.4:p.Gly106=
NR_073520.2:n.1307T>C
NM_001172645.2:c.264T>C	NP_001166116.1:p.Gly88=