The autosomal CFTR gene encodes a transmembrane protein that transports chloride ions across membranes of cells that produce mucus, sweat, tears, saliva and digestive enzymes. A common mutation in this gene delta F508 results in one amino acid being deleted from the protein. This causes the mutant protein to not transport chloride ions as efficiently, so that mucus, sweat, and such are thick and sticky. People homozygous for the mutant allele have cystic fibrosis, but heterozygotes or wild-type homozygotes are unaffected. Select all the terms below that correctly describe this system. HINT: There are FOUR. haplosufficient wildtype allele haploinsufficient wildtype allele gain of function mutation loss of function mutation amorphic mutation hypomorphic mutation hypermorphic mutation neomorphic mutation codominance seen between the two alleles complete dominance seen between the two alleles incomplete dominance seen between the two alleles.