Canonical Allele Identifier: CA8093879

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66550131A>T , CM000678.2:g.66550131A>T	GRCh38
NC_000016.9:g.66584034A>T , CM000678.1:g.66584034A>T	GRCh37
NC_000016.8:g.65141535A>T	NCBI36
NG_016862.1:g.5282T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001172643.1:c.31+122T>A	NP_001166114.1:n.31+122T>A
NM_001172644.1:c.-70T>A	NP_001166115.1:n.-70T>A
NM_001172645.1:c.-70T>A	NP_001166116.1:n.-70T>A
NM_001271934.1:c.-312T>A	NP_001258863.1:n.-312T>A
NM_001271935.1:c.31+122T>A	NP_001258864.1:n.31+122T>A
NM_004614.4:c.-70T>A	NP_004605.4:n.-70T>A
NR_073520.1:n.282T>A
ENST00000299697.11:c.-70T>A	ENSP00000299697.8:n.-70T>A
ENST00000299697.12:c.31+122T>A	ENSP00000299697.9:n.31+122T>A
ENST00000417693.7:c.57T>A	ENSP00000407469.4:p.Ala19=
ENST00000417693.8:c.-70T>A	ENSP00000407469.5:n.-70T>A
ENST00000451102.6:c.57T>A	ENSP00000414334.3:p.Ala19=
ENST00000451102.7:c.31+122T>A	ENSP00000414334.4:n.31+122T>A
ENST00000527284.5:c.31+122T>A	ENSP00000435312.1:n.31+122T>A
ENST00000562484.2:c.-167-1122T>A	ENSP00000463326.1:n.-167-1122T>A
ENST00000563478.5:c.-167-1122T>A	ENSP00000462341.1:n.-167-1122T>A
ENST00000567357.5:c.57T>A	ENSP00000457959.1:p.Ala19=
ENST00000567357.6:c.-70T>A	ENSP00000457959.2:n.-70T>A
ENST00000569718.5:c.18+122T>A
ENST00000569718.6:c.31+122T>A	ENSP00000464313.2:n.31+122T>A
ENST00000620035.4:c.-70T>A	ENSP00000483833.1:n.-70T>A
ENST00000678015.1:c.-167-1122T>A	ENSP00000502959.1:n.-167-1122T>A
ENST00000678297.1:c.-92-1122T>A	ENSP00000503472.1:n.-92-1122T>A
ENST00000678314.1:c.-61+1409T>A	ENSP00000504438.1:n.-61+1409T>A