RHD*34 - RHD*DIM
(ISBT table: RHD partial D v5.0)
				This entry is an RHD allele.
						DIM, DIleM, RHD(C285Y), RHD*854A, RHD*854A (DIM, RHD*34), RHD*854G>A, 
					
	
				Molecular data
						Nucleotides:
						854G>A; 
					
Amino acids: C285Y;
						Hybrid allele encompassing at least one  RHCE  exon:
						no
					
						Comments on the molecular basis:
						
						Extracellular position of one or more amino acid substitutions: 
						
- considered to be extracellular
 - none of the mutations are predicted to affect an extracellular amino acid
 
						Splicing:
						
						Unconventional prediction methods:
						
Phenotype
Main D phenotype: variable/discrepant (last update: Nov. 11, 2019)Reports by D phenotype
Other RH phenotypes: RH:
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
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), in the German population (last update: Feb. 22, 2020)Detailed reports
- 
							1/8442 (1 of the 5 donors who were really weakly D positive) 8442 donors with D negative phenotype, screened for presence of the RHD gene in two surveys; 754 donors were C and/or E positive, the rest were ccee phenotype; 5 donors were revealed to be weakly D positive in the German population (Baden-Wurttemberg), White 
							  (same sample as in 
10753853 ) 
Allele or phenotype frequency
Structure mapping
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References
- Rouillac C et al. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes. Blood, 1995. [Citation] [RHeference]
 - Scott ML et al. A structural model for 30 Rh D epitopes based on serological and DNA sequence data from partial D phenotypes. Transfus Clin Biol, 1996. [Citation] [RHeference]
 - Wagner FF et al. Weak D alleles express distinct phenotypes. Blood, 2000. [Citation] [RHeference]
 - Wagner FF et al. RHD positive haplotypes in D negative Europeans. BMC Genet, 2001. [Citation] [RHeference]
 - Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
 
Last update: Dec. 18, 2019