A novel HLA-A*0119 allele of a Caucasian family containing a mutation in a highly conserved region

Int J Immunogenet. 2006 Aug;33(4):247-8. doi: 10.1111/j.1744-313X.2006.00606.x.

Abstract

A novel human leucocyte antigen (HLA)-A (HLA-A*0119) allele has been identified in two individuals of a Caucasian family from Middle Europe using a single-allele-specific sequencing strategy. This allele is identical to the HLA-A*0101 allele except for one point mutation in the highly conserved codon 92 (TCT --> GCT) resulting in an amino acid change from serine to alanine.

MeSH terms

  • Aged
  • Alleles
  • Amino Acid Substitution
  • Base Sequence
  • Exons
  • Family
  • Female
  • HLA-A Antigens / chemistry
  • HLA-A Antigens / genetics*
  • Humans
  • Leukemia, Myeloid
  • Molecular Sequence Data
  • Point Mutation*
  • Polymerase Chain Reaction
  • White People / genetics

Substances

  • HLA-A Antigens