Canonical Allele Identifier: CA10648722

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66508205C>A , CM000678.2:g.66508205C>A	GRCh38
NC_000016.9:g.66542108C>A , CM000678.1:g.66542108C>A	GRCh37
NC_000016.8:g.65099609C>A	NCBI36
NG_016862.1:g.47208G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544898.6:c.*3763G>T MANE Select	ENSP00000440898.2:n.*3763G>T
ENST00000676821.1:n.122+445G>T
ENST00000677166.1:n.109+3753G>T
ENST00000677319.1:c.676G>T	ENSP00000503900.1:n.676G>T
ENST00000677405.1:n.122+445G>T
ENST00000677535.1:c.2023G>T	ENSP00000502856.1:n.2023G>T
ENST00000677668.1:n.122+445G>T
ENST00000677753.1:n.81+5526G>T
ENST00000678219.1:c.1911G>T	ENSP00000504142.1:n.1911G>T
ENST00000678257.1:n.122+445G>T
ENST00000678282.1:n.82-5198G>T
ENST00000299697.11:c.*3763G>T	ENSP00000299697.8:n.*3763G>T
ENST00000561527.5:n.258+5526G>T
ENST00000561728.1:c.148+5526G>T
ENST00000561905.2:c.620G>T
ENST00000620035.4:c.*3763G>T	ENSP00000483833.1:n.*3763G>T
NM_001172643.1:c.*3763G>T	NP_001166114.1:n.*3763G>T
NM_001172644.1:c.*3763G>T	NP_001166115.1:n.*3763G>T
NM_001172645.1:c.*3763G>T	NP_001166116.1:n.*3763G>T
NM_001271934.1:c.*3763G>T	NP_001258863.1:n.*3763G>T
NM_001271935.1:c.*3858G>T	NP_001258864.1:n.*3858G>T
NM_001272050.1:c.*3763G>T	NP_001258979.1:n.*3763G>T
NM_004614.4:c.*3763G>T	NP_004605.4:n.*3763G>T
NR_073520.1:n.5840G>T
NM_001172644.2:c.*3763G>T	NP_001166115.1:n.*3763G>T
NM_001271934.2:c.*3763G>T	NP_001258863.1:n.*3763G>T
NM_001272050.2:c.*3763G>T	NP_001258979.1:n.*3763G>T
NM_004614.5:c.*3763G>T MANE Select	NP_004605.4:n.*3763G>T
NR_073520.2:n.5550G>T
NM_001172645.2:c.*3763G>T	NP_001166116.1:n.*3763G>T