RHD*643_645delTTC
(ISBT table: not listed)
This entry is an RHD allele.
RHD(215delF), RHD(F215del), RHD*643_645delTTC, RHD*643delTTC or RHD*644delTCT or RHD*645delCTT (215delF), RHD*644_646delTCT, RHD*645_647delCTT,
Molecular data
Nucleotides:
643TTC> ;
Amino acids: F215 (deletion);
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
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:
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: unknown (last update: Dec. 9, 2020)ce | Ce | cE | CE | |
---|---|---|---|---|
ce | 0 | 0 | 0 | 0 |
Ce | 0 | 0 | 0 | |
cE | 0 | 0 | ||
CE | 0 |
Reports by CcEe phenotype
Reports by allele association
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) (last update: Dec. 22, 2019)Structure mapping
Movement | Mouse Input | Touch Input | ||
---|---|---|---|---|
Rotation | Primary Mouse Button | Single touch | ||
Translation | Middle Mouse Button or Ctrl+Primary | Triple touch | ||
Zoom | Scroll Wheel or Second Mouse Button or Shift+Primary | Pinch (double touch) | ||
Slab | Ctrl+Second | Not Available |
References
- L. Tilley et al. Two Novel RhD Variants Caused by Triplet Deletions in the RhD Gene Transfusion Medicine, 2007. — Abstract — [RHeference]
- Sunitha Vege et al. Novel RHD Alleles and Predicting Risk for Anti-D Transfusion, 2020. — Abstract — [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Dec. 10, 2020