A G1789S amino acid replacement (coordinates relative to the cher-PA isoform), along with a PBac{ScarlessHD-DsRed} marker element have been introduced into the endogenous cher locus. The G1789S change is equivalent to a G2299S change in the orthologous human FLNC gene, a variant identified in patients with hypertrophic cardiomyopathy. The presence of the PBac{ScarlessHD-DsRed} marker element introduces a premature stop codon, resulting in a truncated protein deleted from cher residue 1797 (coordinates relative to the cher-PA isoform).