Thec^2jalbino mutation at the mouse tyrosinase locus arose spontaneously in the C57BL/6 inbred strain and causes complete absence of melanin synthesis, as does the “classical”cmutation of long-established albino inbred strains. Sequence analysis ofc^2jcDNA reveals a G → T point mutation at nt 291, causing an arginine → leucine substitution in codon 77, where the arginine position has been conserved in vertebrate tyrosinases and tyrosinase-related proteins. Whilec^2jdiffers fromc,in which there is a G → C mutation at nt 369 causing a cysteine → serine substitution, both mutations change the G1 position of alternative 5′ splice donor sites in exon 1. Bothc^2jandcabolish the usage of the respective sites for alternative splicing of the tyrosinase pre-mRNA in skin melanocytes. Inc^2j,there results an almost eightfold increase in activation of the 5′ splice site located 78 nt downstream, but incthere is no activation of the intact upstream splice site. Although the tyrosinase mRNA levels are similar inc^2jand wildtype, the protein is virtually absent inc^2j,as inc,possibly due to proteolytic degradation.