RHCE*01.37 - RHCE*ce37
(ISBT table: RHCE-15th_July_2019)
This entry is an RHCE allele.
RHCE*ce 697G,712G,733G,744C, RHCE*ce697C>G,712A>G,733C>G,744T>C, RHCE*ce697G,712G,733G,744C (RHCE*ce37),
Molecular data
Nucleotides:
697C>G; 712A>G; 733C>G; 744T>C;
Amino acids: Q233E; M238V; L245V; S248S;
Hybrid allele encompassing at least one RHD exon:
no
Comments on the molecular basis:
- "The cis arrangement of variant sequences in Case 5 was determined by allele-specific polymerase chain reaction (PCR) with primers specific for c.697G and c.744C."
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: variable/discrepant (last update: Dec. 10, 2020)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: ce (last update: Dec. 10, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: expected to be at risk for anti-D (last update: Dec. 10, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), Caucasian (last update: Dec. 10, 2020)Detailed reports
- 1 sample Caucasian
Allele or phenotype frequency
Structure mapping
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References
- International Society of Blood Transfusion et al. International Society of Blood Transfusion (ISBT) allele table Online ressource, 1935. — Online ressource — [RHeference]
- Goldman M et al. Identification of six new RHCE variant alleles in individuals of diverse racial origin. Transfusion, 2016. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Dec. 10, 2020