Canonical Allele Identifier: CA10647909

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66511203A>G , CM000678.2:g.66511203A>G	GRCh38
NC_000016.9:g.66545106A>G , CM000678.1:g.66545106A>G	GRCh37
NC_000016.8:g.65102607A>G	NCBI36
NG_016862.1:g.44210T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.*765T>C	ENSP00000299697.9:n.*765T>C
ENST00000451102.7:c.*765T>C	ENSP00000414334.4:n.*765T>C
ENST00000527284.6:c.1426T>C
ENST00000527800.6:c.*765T>C	ENSP00000433770.1:n.*765T>C
ENST00000544898.6:c.*765T>C MANE Select	ENSP00000440898.2:n.*765T>C
ENST00000567357.6:c.*1421T>C	ENSP00000457959.2:n.*1421T>C
ENST00000620035.5:c.*860T>C	ENSP00000483833.2:n.*860T>C
ENST00000677166.1:n.109+755T>C
ENST00000677319.1:c.109+755T>C	ENSP00000503900.1:n.109+755T>C
ENST00000677420.1:c.*765T>C	ENSP00000504648.1:n.*765T>C
ENST00000677535.1:c.864T>C	ENSP00000502856.1:n.864T>C
ENST00000677555.1:c.*765T>C	ENSP00000503331.1:n.*765T>C
ENST00000677753.1:n.81+2528T>C
ENST00000678015.1:c.*765T>C	ENSP00000502959.1:n.*765T>C
ENST00000678099.1:c.468-254T>C	ENSP00000504701.1:n.468-254T>C
ENST00000678219.1:c.864T>C	ENSP00000504142.1:n.864T>C
ENST00000678282.1:n.81+2528T>C
ENST00000678861.1:c.468-269T>C	ENSP00000502932.1:n.468-269T>C
ENST00000299697.11:c.*765T>C	ENSP00000299697.8:n.*765T>C
ENST00000451102.6:c.*765T>C	ENSP00000414334.3:n.*765T>C
ENST00000527284.5:c.*765T>C	ENSP00000435312.1:n.*765T>C
ENST00000527800.5:c.*765T>C	ENSP00000433770.1:n.*765T>C
ENST00000544898.5:c.*765T>C	ENSP00000440898.2:n.*765T>C
ENST00000561527.5:n.258+2528T>C
ENST00000561728.1:c.148+2528T>C
ENST00000561905.2:c.54-2432T>C
ENST00000567357.5:c.*1421T>C	ENSP00000457959.1:n.*1421T>C
ENST00000568170.1:n.50T>C
ENST00000620035.4:c.*765T>C	ENSP00000483833.1:n.*765T>C
NM_001172643.1:c.*765T>C	NP_001166114.1:n.*765T>C
NM_001172644.1:c.*765T>C	NP_001166115.1:n.*765T>C
NM_001172645.1:c.*765T>C	NP_001166116.1:n.*765T>C
NM_001271934.1:c.*765T>C	NP_001258863.1:n.*765T>C
NM_001271935.1:c.*860T>C	NP_001258864.1:n.*860T>C
NM_001272050.1:c.*765T>C	NP_001258979.1:n.*765T>C
NM_004614.4:c.*765T>C	NP_004605.4:n.*765T>C
NR_073520.1:n.2842T>C
NM_001172644.2:c.*765T>C	NP_001166115.1:n.*765T>C
NM_001271934.2:c.*765T>C	NP_001258863.1:n.*765T>C
NM_001272050.2:c.*765T>C	NP_001258979.1:n.*765T>C
NM_004614.5:c.*765T>C MANE Select	NP_004605.4:n.*765T>C
NR_073520.2:n.2552T>C
NM_001172645.2:c.*765T>C	NP_001166116.1:n.*765T>C