DIVa cluster

DesignationISBT nameHaplotypePhenotypeMechanismAlterationsFirst mentionDefinitive publication
Ccdes-1RHD*03N.01
CcdeD negativeComplex changes1006G>T (G336C)
186G>T (L62F)
410C>T (A137V)
455A>C (N152T)
Hybrid RHCE[245V](4-7)
20042004
Ccdes-2RHD*01N.06
CcdeD negativehybrid allele1006G>T (G336C)
Hybrid RHCE[245V](4-7)
20092009
D-SPMRHD*40
RHD*D-SPM
cDePartial DMultiple missense mutations186G>T (L62F)
410C>T (A137V)
455A>C (N152T)
509T>C (M170T)
667T>G (F223V)
2012
D186Tnot reportedSingle missense mutation186G>T (L62F)
2012
DIII type 4RHD*03.04
RHD*DIII.4
CDePartial D
D category
hybrid allele186G>T (L62F)
410C>T (A137V)
455A>C (N152T)
20002000
DIII type 5RHD*03.01
RHD*DIIIa
cDePartial D
D category
Multiple missense mutations186G>T (L62F)
410C>T (A137V)
455A>C (N152T)
602C>G (T201R)
667T>G (F223V)
819G>A
DIII type 6RHD*03.06
RHD*DIII.6
cDePartial D
D category
Multiple missense mutations410C>T (A137V)
455A>C (N152T)
602C>G (T201R)
667T>G (F223V)
819G>A
20052006
DIII type 7RHD*03.07
RHD*DIII.07
cDePartial D
D category
Complex changes410C>T (A137V)
455A>C (N152T)
602C>G (T201R)
667T>G (F223V)
819G>A
Hybrid RHCE(2)
20052006
DIII type 8RHD*03.08
RHD*DIII.08
not reportedPartial D
D category
Multiple missense mutations410C>T (A137V)
455A>C (N152T)
2010
DIIIa150Cnot reportedMultiple missense mutations150T>C
186G>T (L62F)
410C>T (A137V)
455A>C (N152T)
602C>G (T201R)
667T>G (F223V)
819G>A
2012
DIV(S103P)cDeMultiple missense mutations186G>T (L62F)
307T>C (S103P)
410C>T (A137V)
455A>C (N152T)
2013
DIV type 1.0RHD*04.01
RHD*DIVa.
cDePartial D
D category
Multiple missense mutations1048G>C (D350H)
186G>T (L62F)
410C>T (A137V)
455A>C (N152T)
2012