Canonical Allele Identifier: CA16608214

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66550317A>T , CM000678.2:g.66550317A>T	GRCh38
NC_000016.9:g.66584220A>T , CM000678.1:g.66584220A>T	GRCh37
NC_000016.8:g.65141721A>T	NCBI36
NG_016862.1:g.5096T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001172644.1:c.-256T>A	NP_001166115.1:n.-256T>A
NM_001172645.1:c.-256T>A	NP_001166116.1:n.-256T>A
NM_001271934.1:c.-498T>A	NP_001258863.1:n.-498T>A
NM_004614.4:c.-256T>A	NP_004605.4:n.-256T>A
NR_073520.1:n.96T>A
ENST00000299697.11:c.-256T>A	ENSP00000299697.8:n.-256T>A
ENST00000451102.6:c.-130T>A	ENSP00000414334.3:n.-130T>A
ENST00000451102.7:c.-34T>A	ENSP00000414334.4:n.-34T>A
ENST00000562484.2:c.-167-1308T>A	ENSP00000463326.1:n.-167-1308T>A
ENST00000563478.5:c.-168+1223T>A	ENSP00000462341.1:n.-168+1223T>A
ENST00000569718.6:c.-34T>A	ENSP00000464313.2:n.-34T>A
ENST00000620035.4:c.-256T>A	ENSP00000483833.1:n.-256T>A
ENST00000678015.1:c.-168+1095T>A	ENSP00000502959.1:n.-168+1095T>A
ENST00000678297.1:c.-93+1095T>A	ENSP00000503472.1:n.-93+1095T>A
ENST00000678314.1:c.-61+1223T>A	ENSP00000504438.1:n.-61+1223T>A