Canonical Allele Identifier: CA396194350

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66550031C>T , CM000678.2:g.66550031C>T	GRCh38
NC_000016.9:g.66583934C>T , CM000678.1:g.66583934C>T	GRCh37
NC_000016.8:g.65141435C>T	NCBI36
NG_016862.1:g.5382G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.31+222G>A	ENSP00000299697.9:n.31+222G>A
ENST00000417693.8:c.31G>A	ENSP00000407469.5:p.Ala11Thr
ENST00000451102.7:c.31+222G>A	ENSP00000414334.4:n.31+222G>A
ENST00000544898.6:c.31G>A MANE Select	ENSP00000440898.2:p.Ala11Thr
ENST00000567357.6:c.31G>A	ENSP00000457959.2:p.Ala11Thr
ENST00000569718.6:c.31+222G>A	ENSP00000464313.2:n.31+222G>A
ENST00000620035.5:c.31G>A	ENSP00000483833.2:p.Ala11Thr
ENST00000677420.1:c.-1135G>A	ENSP00000504648.1:n.-1135G>A
ENST00000678015.1:c.-167-1022G>A	ENSP00000502959.1:n.-167-1022G>A
ENST00000678297.1:c.-92-1022G>A	ENSP00000503472.1:n.-92-1022G>A
ENST00000678314.1:c.-61+1509G>A	ENSP00000504438.1:n.-61+1509G>A
ENST00000679327.1:n.74G>A
ENST00000299697.11:c.31G>A	ENSP00000299697.8:p.Ala11Thr
ENST00000417693.7:c.157G>A	ENSP00000407469.4:p.Ala53Thr
ENST00000451102.6:c.157G>A	ENSP00000414334.3:p.Ala53Thr
ENST00000527284.5:c.31+222G>A	ENSP00000435312.1:n.31+222G>A
ENST00000544898.5:c.31G>A	ENSP00000440898.2:p.Ala11Thr
ENST00000545043.6:c.31G>A	ENSP00000438143.2:p.Ala11Thr
ENST00000562484.2:c.-167-1022G>A	ENSP00000463326.1:n.-167-1022G>A
ENST00000563478.5:c.-167-1022G>A	ENSP00000462341.1:n.-167-1022G>A
ENST00000564917.5:c.31G>A	ENSP00000455187.1:p.Ala11Thr
ENST00000567357.5:c.157G>A	ENSP00000457959.1:p.Ala53Thr
ENST00000569718.5:c.18+222G>A
ENST00000620035.4:c.31G>A	ENSP00000483833.1:p.Ala11Thr
NM_001172643.1:c.31+222G>A	NP_001166114.1:n.31+222G>A
NM_001172644.1:c.31G>A	NP_001166115.1:p.Ala11Thr
NM_001172645.1:c.31G>A	NP_001166116.1:p.Ala11Thr
NM_001271934.1:c.-212G>A	NP_001258863.1:n.-212G>A
NM_001271935.1:c.31+222G>A	NP_001258864.1:n.31+222G>A
NM_004614.4:c.31G>A	NP_004605.4:p.Ala11Thr
NR_073520.1:n.382G>A
NM_001172644.2:c.31G>A	NP_001166115.1:p.Ala11Thr
NM_001271934.2:c.-212G>A	NP_001258863.1:n.-212G>A
NM_001272050.2:c.-622G>A	NP_001258979.1:n.-622G>A
NM_004614.5:c.31G>A MANE Select	NP_004605.4:p.Ala11Thr
NR_073520.2:n.92G>A
NM_001172645.2:c.31G>A	NP_001166116.1:p.Ala11Thr