Canonical Allele Identifier: CA495905501

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66562962A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66529059A>G , CM000678.2:g.66529059A>G	GRCh38
NC_000016.9:g.66562962A>G , CM000678.1:g.66562962A>G	GRCh37
NC_000016.8:g.65120463A>G	NCBI36
NG_016862.1:g.26354T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.216T>C	ENSP00000299697.9:p.Ser72=
ENST00000417693.8:c.330T>C	ENSP00000407469.5:p.Ser110=
ENST00000451102.7:c.291T>C	ENSP00000414334.4:p.Ser97=
ENST00000527284.6:c.328T>C
ENST00000527800.6:c.93T>C	ENSP00000433770.1:p.Ser31=
ENST00000544898.6:c.384T>C MANE Select	ENSP00000440898.2:p.Ser128=
ENST00000567357.6:c.*242T>C	ENSP00000457959.2:n.*242T>C
ENST00000569718.6:c.291T>C	ENSP00000464313.2:p.Ser97=
ENST00000620035.5:c.309T>C	ENSP00000483833.2:p.Ser103=
ENST00000676538.1:c.33-11182T>C
ENST00000677379.1:c.90+2321T>C	ENSP00000503672.1:n.90+2321T>C
ENST00000677420.1:c.93T>C	ENSP00000504648.1:p.Ser31=
ENST00000677555.1:c.93T>C	ENSP00000503331.1:p.Ser31=
ENST00000677715.1:c.93T>C	ENSP00000502950.1:p.Ser31=
ENST00000677739.1:c.63T>C	ENSP00000504644.1:p.Ser21=
ENST00000678015.1:c.93T>C	ENSP00000502959.1:p.Ser31=
ENST00000678297.1:c.93T>C	ENSP00000503472.1:p.Ser31=
ENST00000678314.1:c.93T>C	ENSP00000504438.1:p.Ser31=
ENST00000678746.1:c.274T>C	ENSP00000503227.1:n.274T>C
ENST00000299697.11:c.384T>C	ENSP00000299697.8:p.Ser128=
ENST00000417693.7:c.456T>C	ENSP00000407469.4:p.Ser152=
ENST00000451102.6:c.510T>C	ENSP00000414334.3:p.Ser170=
ENST00000525974.5:c.93T>C	ENSP00000434594.1:p.Ser31=
ENST00000527284.5:c.291T>C	ENSP00000435312.1:p.Ser97=
ENST00000527800.5:c.93T>C	ENSP00000433770.1:p.Ser31=
ENST00000544898.5:c.384T>C	ENSP00000440898.2:p.Ser128=
ENST00000545043.6:c.309T>C	ENSP00000438143.2:p.Ser103=
ENST00000562484.2:c.93T>C	ENSP00000463326.1:p.Ser31=
ENST00000563369.6:c.93T>C	ENSP00000463560.1:p.Ser31=
ENST00000563478.5:c.93T>C	ENSP00000462341.1:p.Ser31=
ENST00000564917.5:c.384T>C	ENSP00000455187.1:p.Ser128=
ENST00000567357.5:c.*242T>C	ENSP00000457959.1:n.*242T>C
ENST00000569718.5:c.278T>C
ENST00000620035.4:c.330T>C	ENSP00000483833.1:p.Ser110=
NM_001172643.1:c.291T>C	NP_001166114.1:p.Ser97=
NM_001172644.1:c.309T>C	NP_001166115.1:p.Ser103=
NM_001172645.1:c.330T>C	NP_001166116.1:p.Ser110=
NM_001271934.1:c.237T>C	NP_001258863.1:p.Ser79=
NM_001271935.1:c.291T>C	NP_001258864.1:p.Ser97=
NM_001272050.1:c.93T>C	NP_001258979.1:p.Ser31=
NM_004614.4:c.384T>C	NP_004605.4:p.Ser128=
NR_073520.1:n.1663T>C
NM_001172644.2:c.309T>C	NP_001166115.1:p.Ser103=
NM_001271934.2:c.237T>C	NP_001258863.1:p.Ser79=
NM_001272050.2:c.93T>C	NP_001258979.1:p.Ser31=
NM_004614.5:c.384T>C MANE Select	NP_004605.4:p.Ser128=
NR_073520.2:n.1373T>C
NM_001172645.2:c.330T>C	NP_001166116.1:p.Ser110=