Canonical Allele Identifier: CA396190626

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66565336T>A (hg19) ; chr16:g.66531433T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531433T>A , CM000678.2:g.66531433T>A	GRCh38
NC_000016.9:g.66565336T>A , CM000678.1:g.66565336T>A	GRCh37
NC_000016.8:g.65122837T>A	NCBI36
NG_016862.1:g.23980A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.154A>T	ENSP00000299697.9:p.Thr52Ser
ENST00000417693.8:c.268A>T	ENSP00000407469.5:p.Thr90Ser
ENST00000451102.7:c.229A>T	ENSP00000414334.4:p.Thr77Ser
ENST00000527284.6:c.266A>T
ENST00000527800.6:c.31A>T	ENSP00000433770.1:p.Thr11Ser
ENST00000544898.6:c.322A>T MANE Select	ENSP00000440898.2:p.Thr108Ser
ENST00000567357.6:c.*180A>T	ENSP00000457959.2:n.*180A>T
ENST00000569718.6:c.229A>T	ENSP00000464313.2:p.Thr77Ser
ENST00000620035.5:c.247A>T	ENSP00000483833.2:p.Thr83Ser
ENST00000676538.1:c.33-13556A>T
ENST00000677379.1:c.37A>T	ENSP00000503672.1:p.Thr13Ser
ENST00000677420.1:c.31A>T	ENSP00000504648.1:p.Thr11Ser
ENST00000677497.1:n.209A>T
ENST00000677555.1:c.31A>T	ENSP00000503331.1:p.Thr11Ser
ENST00000677715.1:c.31A>T	ENSP00000502950.1:p.Thr11Ser
ENST00000677739.1:c.55-2366A>T	ENSP00000504644.1:n.55-2366A>T
ENST00000678015.1:c.31A>T	ENSP00000502959.1:p.Thr11Ser
ENST00000678297.1:c.31A>T	ENSP00000503472.1:p.Thr11Ser
ENST00000678314.1:c.31A>T	ENSP00000504438.1:p.Thr11Ser
ENST00000678746.1:c.212A>T	ENSP00000503227.1:n.212A>T
ENST00000679154.1:c.69A>T
ENST00000299697.11:c.322A>T	ENSP00000299697.8:p.Thr108Ser
ENST00000417693.7:c.394A>T	ENSP00000407469.4:p.Thr132Ser
ENST00000451102.6:c.448A>T	ENSP00000414334.3:p.Thr150Ser
ENST00000525974.5:c.31A>T	ENSP00000434594.1:p.Thr11Ser
ENST00000527284.5:c.229A>T	ENSP00000435312.1:p.Thr77Ser
ENST00000527800.5:c.31A>T	ENSP00000433770.1:p.Thr11Ser
ENST00000544898.5:c.322A>T	ENSP00000440898.2:p.Thr108Ser
ENST00000545043.6:c.247A>T	ENSP00000438143.2:p.Thr83Ser
ENST00000562484.2:c.31A>T	ENSP00000463326.1:p.Thr11Ser
ENST00000563369.6:c.31A>T	ENSP00000463560.1:p.Thr11Ser
ENST00000563478.5:c.31A>T	ENSP00000462341.1:p.Thr11Ser
ENST00000564917.5:c.322A>T	ENSP00000455187.1:p.Thr108Ser
ENST00000567357.5:c.*180A>T	ENSP00000457959.1:n.*180A>T
ENST00000569718.5:c.216A>T
ENST00000620035.4:c.268A>T	ENSP00000483833.1:p.Thr90Ser
NM_001172643.1:c.229A>T	NP_001166114.1:p.Thr77Ser
NM_001172644.1:c.247A>T	NP_001166115.1:p.Thr83Ser
NM_001172645.1:c.268A>T	NP_001166116.1:p.Thr90Ser
NM_001271934.1:c.175A>T	NP_001258863.1:p.Thr59Ser
NM_001271935.1:c.229A>T	NP_001258864.1:p.Thr77Ser
NM_001272050.1:c.31A>T	NP_001258979.1:p.Thr11Ser
NM_004614.4:c.322A>T	NP_004605.4:p.Thr108Ser
NR_073520.1:n.1601A>T
NM_001172644.2:c.247A>T	NP_001166115.1:p.Thr83Ser
NM_001271934.2:c.175A>T	NP_001258863.1:p.Thr59Ser
NM_001272050.2:c.31A>T	NP_001258979.1:p.Thr11Ser
NM_004614.5:c.322A>T MANE Select	NP_004605.4:p.Thr108Ser
NR_073520.2:n.1311A>T
NM_001172645.2:c.268A>T	NP_001166116.1:p.Thr90Ser