The t(9;22) (BCR/ABL) and t(4;11) (AF4/MLL) positivity suggests a poor prognosis in B-acute lymphoblastic leukemia (ALL). Many western studies have highlighted the frequency and profile of BCR-ABL-positive B-ALL; however, data from the Indian subcontinent is limited. The aim of the pilot study is to present the complete clinicohematological, immunophenotyping, and molecular profile of BCR-ABL-positive B-ALL. It is a prospective study involving a total of 15 BCR-ABL-positive B-ALL cases diagnosed by bone marrow examination, immunophenotyping, and multiplex reverse transcriptase polymerase chain reaction assay in our institute. Out of the total 15 cases enrolled in the study, ten (67 %) were adult and five (33 %), pediatric. All cases had splenomegaly, hepatomegaly, high WBC count (>20×10 9 /L), and low platelet count (<100×10 9 /L) at presentation. Twelve of 15 (80 %) showed aberrant myeloid marker expression, of which 11 showed expression of two myeloid antigens (CD13 and CD117/33). The BCR-ABL transcript type in our study was p210 seen in 8/15 (53.3 %) cases, while p190 in 7/15 (46.6 %) cases. Thirteen of 15 (87 %) cases received imatinib in addition to the ALL induction regimen. Ten of 13 (77 %) of these had complete hematological remission at first check marrow. The disease-free interval, however, ranged from 4-6 months in 6/15 (40 %) cases. Analysis for BCR-ABL transcript is necessary in B-ALL as the cases may benefit from addition of imatinib to the treatment regimen.