| Designation | ISBT name | Haplotype | Phenotype | Mechanism | Alterations | First mention | Definitive publication |
| Ccdes-1 | RHD*03N.01 | Ccde | D negative | Complex changes | 1006G>T (G336C) 186G>T (L62F) 410C>T (A137V) 455A>C (N152T) Hybrid RHCE[245V](4-7) | 2004 | 2004 |
| Ccdes-2 | RHD*01N.06 | Ccde | D negative | hybrid allele | 1006G>T (G336C) Hybrid RHCE[245V](4-7) | 2009 | 2009 |
| D-SPM | RHD*40 RHD*D-SPM | cDe | Partial D | Multiple missense mutations | 186G>T (L62F) 410C>T (A137V) 455A>C (N152T) 509T>C (M170T) 667T>G (F223V) | 2012 | |
| D186T | not reported | Single missense mutation | 186G>T (L62F) | 2012 | |||
| DIII type 4 | RHD*03.04 RHD*DIII.4 | CDe | Partial D D category | hybrid allele | 186G>T (L62F) 410C>T (A137V) 455A>C (N152T) | 2000 | 2000 |
| DIII type 5 | RHD*03.01 RHD*DIIIa | cDe | Partial D D category | Multiple missense mutations | 186G>T (L62F) 410C>T (A137V) 455A>C (N152T) 602C>G (T201R) 667T>G (F223V) 819G>A | ||
| DIII type 6 | RHD*03.06 RHD*DIII.6 | cDe | Partial D D category | Multiple missense mutations | 410C>T (A137V) 455A>C (N152T) 602C>G (T201R) 667T>G (F223V) 819G>A | 2005 | 2006 |
| DIII type 7 | RHD*03.07 RHD*DIII.07 | cDe | Partial D D category | Complex changes | 410C>T (A137V) 455A>C (N152T) 602C>G (T201R) 667T>G (F223V) 819G>A Hybrid RHCE(2) | 2005 | 2006 |
| DIII type 8 | RHD*03.08 RHD*DIII.08 | not reported | Partial D D category | Multiple missense mutations | 410C>T (A137V) 455A>C (N152T) | 2010 | |
| DIII type 9 | RHD*03.09 RHD*DIII.09 | not reported | Partial D | Multiple missense mutations | 186G>T (L62F) 410C>T (A137V) 455A>C (N152T) 667T>G (F223V) | ||
| DIIIa-ceS(1-2)-D(3)-ceS(4-7)-D | not reported | hybrid allele | 1006G>T (G336C) 410C>T (A137V) 455A>C (N152T) 48G>C (W16C) Hybrid RHCE(2) Hybrid RHCE[245V](4-7) | 2017 | |||
| DIIIa150C | not reported | Multiple missense mutations | 150T>C 186G>T (L62F) 410C>T (A137V) 455A>C (N152T) 602C>G (T201R) 667T>G (F223V) 819G>A | 2012 | |||
| DIV(S103P) | cDe | Multiple missense mutations | 186G>T (L62F) 307T>C (S103P) 410C>T (A137V) 455A>C (N152T) | 2013 | |||
| DIV type 1.0 | RHD*04.01 RHD*DIVa. | cDe | Partial D D category | Multiple missense mutations | 1048G>C (D350H) 186G>T (L62F) 410C>T (A137V) 455A>C (N152T) | 2012 | |
| DOL-4 | RHD*12.04 RHD*DOL4 | not reported | Partial D | hybrid allele | 410C>T (A137V) 455A>C (N152T) 509T>C (M170T) 667T>G (F223V) | ||
| RHD(A137V,N152T)-CE(4-6)-D(7-10) | not reported | hybrid allele | 410C>T (A137V) 455A>C (N152T) Hybrid RHCE(4-6) | 2016 |