Abstract
We detected a rare HLA-A*24:137 allele in an unrelated Taiwanese haematopoietic stem cell donor during a routine SBT (sequence-based typing) HLA typing exercise. The DNA sequence of A*24:137 is identical to the sequence of A*24:02:01:01 in exons 2 and 3 except at codon 21 where CGC was replaced with CAA. The DNA variation caused an amino acid alteration at amino acid residue 21 (R->Q). The HLA haplotype in association with A*24:137 may be deduced as A*24:137-B*15-DRB1*14. The formation of A*24:137 was probably the result of a nucleotide point mutation involving A*24:02:01:01. It remains to be determined whether A*24:137 is restricted to Taiwanese/Chinese ethnicity.
Original language | English |
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Pages (from-to) | 530-531 |
Number of pages | 2 |
Journal | International Journal of Immunogenetics |
Volume | 39 |
Issue number | 6 |
DOIs | |
Publication status | Published - Dec 1 2012 |
Externally published | Yes |
ASJC Scopus subject areas
- Genetics
- Molecular Biology
- Immunology
- Genetics(clinical)