Canonical Allele Identifier: CA396193359

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66582911A>T (hg19) ; chr16:g.66549008A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66549008A>T , CM000678.2:g.66549008A>T	GRCh38
NC_000016.9:g.66582911A>T , CM000678.1:g.66582911A>T	GRCh37
NC_000016.8:g.65140412A>T	NCBI36
NG_016862.1:g.6405T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.33T>A	ENSP00000299697.9:p.Asp11Glu
ENST00000417693.8:c.126T>A	ENSP00000407469.5:p.Asp42Glu
ENST00000451102.7:c.33T>A	ENSP00000414334.4:p.Asp11Glu
ENST00000527284.6:c.70T>A
ENST00000527800.6:c.-166T>A	ENSP00000433770.1:n.-166T>A
ENST00000544898.6:c.126T>A MANE Select	ENSP00000440898.2:p.Asp42Glu
ENST00000567357.6:c.126T>A	ENSP00000457959.2:p.Asp42Glu
ENST00000569718.6:c.33T>A	ENSP00000464313.2:p.Asp11Glu
ENST00000620035.5:c.126T>A	ENSP00000483833.2:p.Asp42Glu
ENST00000676536.1:c.2T>A
ENST00000676538.1:c.2T>A
ENST00000677124.1:n.2T>A
ENST00000677412.1:c.2T>A
ENST00000677420.1:c.-112T>A	ENSP00000504648.1:n.-112T>A
ENST00000677541.1:c.2T>A
ENST00000677555.1:c.-91T>A	ENSP00000503331.1:n.-91T>A
ENST00000677715.1:c.-166T>A	ENSP00000502950.1:n.-166T>A
ENST00000678015.1:c.-166T>A	ENSP00000502959.1:n.-166T>A
ENST00000678205.1:c.2T>A
ENST00000678297.1:c.-91T>A	ENSP00000503472.1:n.-91T>A
ENST00000678314.1:c.-61+2532T>A	ENSP00000504438.1:n.-61+2532T>A
ENST00000679154.1:c.2T>A
ENST00000679271.1:n.32T>A
ENST00000679327.1:n.1097T>A
ENST00000299697.11:c.126T>A	ENSP00000299697.8:p.Asp42Glu
ENST00000417693.7:c.252T>A	ENSP00000407469.4:p.Asp84Glu
ENST00000451102.6:c.252T>A	ENSP00000414334.3:p.Asp84Glu
ENST00000525974.5:c.-166T>A	ENSP00000434594.1:n.-166T>A
ENST00000527284.5:c.33T>A	ENSP00000435312.1:p.Asp11Glu
ENST00000527800.5:c.-166T>A	ENSP00000433770.1:n.-166T>A
ENST00000544898.5:c.126T>A	ENSP00000440898.2:p.Asp42Glu
ENST00000545043.6:c.126T>A	ENSP00000438143.2:p.Asp42Glu
ENST00000562484.2:c.-166T>A	ENSP00000463326.1:n.-166T>A
ENST00000563369.6:c.-166T>A	ENSP00000463560.1:n.-166T>A
ENST00000563478.5:c.-166T>A	ENSP00000462341.1:n.-166T>A
ENST00000564917.5:c.126T>A	ENSP00000455187.1:p.Asp42Glu
ENST00000567357.5:c.252T>A	ENSP00000457959.1:p.Asp84Glu
ENST00000569718.5:c.20T>A
ENST00000620035.4:c.126T>A	ENSP00000483833.1:p.Asp42Glu
NM_001172643.1:c.33T>A	NP_001166114.1:p.Asp11Glu
NM_001172644.1:c.126T>A	NP_001166115.1:p.Asp42Glu
NM_001172645.1:c.126T>A	NP_001166116.1:p.Asp42Glu
NM_001271934.1:c.-117T>A	NP_001258863.1:n.-117T>A
NM_001271935.1:c.33T>A	NP_001258864.1:p.Asp11Glu
NM_001272050.1:c.-166T>A	NP_001258979.1:n.-166T>A
NM_004614.4:c.126T>A	NP_004605.4:p.Asp42Glu
NR_073520.1:n.1405T>A
NM_001172644.2:c.126T>A	NP_001166115.1:p.Asp42Glu
NM_001271934.2:c.-117T>A	NP_001258863.1:n.-117T>A
NM_001272050.2:c.-166T>A	NP_001258979.1:n.-166T>A
NM_004614.5:c.126T>A MANE Select	NP_004605.4:p.Asp42Glu
NR_073520.2:n.1115T>A
NM_001172645.2:c.126T>A	NP_001166116.1:p.Asp42Glu