Canonical Allele Identifier: CA10638185
Gene: TK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 320130
ClinVar RCV Id: RCV000407947
dbSNP Id: rs886052195

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.66510209_66510210insAA , CM000678.2:g.66510209_66510210insAA GRCh38
NC_000016.9:g.66544112_66544113insAA , CM000678.1:g.66544112_66544113insAA GRCh37
NC_000016.8:g.65101613_65101614insAA NCBI36
NG_016862.1:g.45203_45204insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000299697.12:c.*1758_*1759insTT ENSP00000299697.9:n.*1758_*1759insTT
ENST00000451102.7:c.*1758_*1759insTT ENSP00000414334.4:n.*1758_*1759insTT
ENST00000544898.6:c.*1758_*1759insTT MANE Select ENSP00000440898.2:n.*1758_*1759insTT
ENST00000620035.5:c.*1853_*1854insTT ENSP00000483833.2:n.*1853_*1854insTT
ENST00000677166.1:n.109+1748_109+1749insTT
ENST00000677319.1:c.110-1439_110-1438insTT ENSP00000503900.1:n.110-1439_110-1438insTT
ENST00000677535.1:c.1456+401_1456+402insTT ENSP00000502856.1:n.1456+401_1456+402insTT
ENST00000677753.1:n.81+3521_81+3522insTT
ENST00000678015.1:c.*1758_*1759insTT ENSP00000502959.1:n.*1758_*1759insTT
ENST00000678099.1:c.1207_1208insTT ENSP00000504701.1:n.1207_1208insTT
ENST00000678219.1:c.1344+513_1344+514insTT ENSP00000504142.1:n.1344+513_1344+514insTT
ENST00000678282.1:n.81+3521_81+3522insTT
ENST00000678861.1:c.1192_1193insTT ENSP00000502932.1:n.1192_1193insTT
ENST00000299697.11:c.*1758_*1759insTT ENSP00000299697.8:n.*1758_*1759insTT
ENST00000451102.6:c.*1758_*1759insTT ENSP00000414334.3:n.*1758_*1759insTT
ENST00000544898.5:c.*1758_*1759insTT ENSP00000440898.2:n.*1758_*1759insTT
ENST00000561527.5:n.258+3521_258+3522insTT
ENST00000561728.1:c.148+3521_148+3522insTT
ENST00000561905.2:c.54-1439_54-1438insTT
ENST00000620035.4:c.*1758_*1759insTT ENSP00000483833.1:n.*1758_*1759insTT
NM_001172643.1:c.*1758_*1759insTT NP_001166114.1:n.*1758_*1759insTT
NM_001172644.1:c.*1758_*1759insTT NP_001166115.1:n.*1758_*1759insTT
NM_001172645.1:c.*1758_*1759insTT NP_001166116.1:n.*1758_*1759insTT
NM_001271934.1:c.*1758_*1759insTT NP_001258863.1:n.*1758_*1759insTT
NM_001271935.1:c.*1853_*1854insTT NP_001258864.1:n.*1853_*1854insTT
NM_001272050.1:c.*1758_*1759insTT NP_001258979.1:n.*1758_*1759insTT
NM_004614.4:c.*1758_*1759insTT NP_004605.4:n.*1758_*1759insTT
NR_073520.1:n.3835_3836insTT
NM_001172644.2:c.*1758_*1759insTT NP_001166115.1:n.*1758_*1759insTT
NM_001271934.2:c.*1758_*1759insTT NP_001258863.1:n.*1758_*1759insTT
NM_001272050.2:c.*1758_*1759insTT NP_001258979.1:n.*1758_*1759insTT
NM_004614.5:c.*1758_*1759insTT MANE Select NP_004605.4:n.*1758_*1759insTT
NR_073520.2:n.3545_3546insTT
NM_001172645.2:c.*1758_*1759insTT NP_001166116.1:n.*1758_*1759insTT