RHD*329C,1054A
(ISBT table: not listed)
This entry is an RHD allele.
RHD(L110P,V352I), RHD(V352I), RHD*329C,1054A, RHD*329T>C,1054G>A,
Molecular data
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
- only mentions c.1054G>A
- corresponding author was contacted and confirmed the presence of both mutations in cis in the sample
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: variable/discrepant (last update: Nov. 17, 2019)Reports by D phenotype
Other RH phenotypes: RH:-3,
- RH:-3 inferred from the reported RHCE phenotypes of the carriers
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: Ce? (last update: Dec. 9, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Nov. 17, 2019)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), North African (last update: Dec. 22, 2019)Structure mapping
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Slab | Ctrl+Second | Not Available |
References
- Wagner FF and Flegel WA et al. The Human RhesusBase Online ressource, 2011. — Online ressource — [RHeference]
- Fichou Y et al. Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare alleles. Transfusion, 2013. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Feb. 25, 2020