Canonical Allele Identifier: CA10647903

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66510228_66510229insG , CM000678.2:g.66510228_66510229insG	GRCh38
NC_000016.9:g.66544131_66544132insG , CM000678.1:g.66544131_66544132insG	GRCh37
NC_000016.8:g.65101632_65101633insG	NCBI36
NG_016862.1:g.45184_45185insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.*1739_*1740insC	ENSP00000299697.9:n.*1739_*1740insC
ENST00000451102.7:c.*1739_*1740insC	ENSP00000414334.4:n.*1739_*1740insC
ENST00000544898.6:c.*1739_*1740insC MANE Select	ENSP00000440898.2:n.*1739_*1740insC
ENST00000620035.5:c.*1834_*1835insC	ENSP00000483833.2:n.*1834_*1835insC
ENST00000677166.1:n.109+1729_109+1730insC
ENST00000677319.1:c.110-1458_110-1457insC	ENSP00000503900.1:n.110-1458_110-1457insC
ENST00000677535.1:c.1456+382_1456+383insC	ENSP00000502856.1:n.1456+382_1456+383insC
ENST00000677753.1:n.81+3502_81+3503insC
ENST00000678015.1:c.*1739_*1740insC	ENSP00000502959.1:n.*1739_*1740insC
ENST00000678099.1:c.1188_1189insC	ENSP00000504701.1:n.1188_1189insC
ENST00000678219.1:c.1344+494_1344+495insC	ENSP00000504142.1:n.1344+494_1344+495insC
ENST00000678282.1:n.81+3502_81+3503insC
ENST00000678861.1:c.1173_1174insC	ENSP00000502932.1:n.1173_1174insC
ENST00000299697.11:c.*1739_*1740insC	ENSP00000299697.8:n.*1739_*1740insC
ENST00000451102.6:c.*1739_*1740insC	ENSP00000414334.3:n.*1739_*1740insC
ENST00000544898.5:c.*1739_*1740insC	ENSP00000440898.2:n.*1739_*1740insC
ENST00000561527.5:n.258+3502_258+3503insC
ENST00000561728.1:c.148+3502_148+3503insC
ENST00000561905.2:c.54-1458_54-1457insC
ENST00000620035.4:c.*1739_*1740insC	ENSP00000483833.1:n.*1739_*1740insC
NM_001172643.1:c.*1739_*1740insC	NP_001166114.1:n.*1739_*1740insC
NM_001172644.1:c.*1739_*1740insC	NP_001166115.1:n.*1739_*1740insC
NM_001172645.1:c.*1739_*1740insC	NP_001166116.1:n.*1739_*1740insC
NM_001271934.1:c.*1739_*1740insC	NP_001258863.1:n.*1739_*1740insC
NM_001271935.1:c.*1834_*1835insC	NP_001258864.1:n.*1834_*1835insC
NM_001272050.1:c.*1739_*1740insC	NP_001258979.1:n.*1739_*1740insC
NM_004614.4:c.*1739_*1740insC	NP_004605.4:n.*1739_*1740insC
NR_073520.1:n.3816_3817insC
NM_001172644.2:c.*1739_*1740insC	NP_001166115.1:n.*1739_*1740insC
NM_001271934.2:c.*1739_*1740insC	NP_001258863.1:n.*1739_*1740insC
NM_001272050.2:c.*1739_*1740insC	NP_001258979.1:n.*1739_*1740insC
NM_004614.5:c.*1739_*1740insC MANE Select	NP_004605.4:n.*1739_*1740insC
NR_073520.2:n.3526_3527insC
NM_001172645.2:c.*1739_*1740insC	NP_001166116.1:n.*1739_*1740insC