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. 2004 Dec 15;32(22):6557–6564. doi: 10.1093/nar/gkh967

Table 6. HPRT cryptic splice sites.

  Legitimate splice site Cryptic splice site Splice variant
Cryptic donor splice sites
Intron
 1* GTG/g1704tgagc cag1752/gtggcg Inclusion of 1–49 of intron 1
 5* GAA/g31635taagt Aag31701/gtaagc Inclusion of 1–67 of intron 5
Cryptic acceptor splice sites
Exon
 2 tttcag14779/A28TT TAG32/T Skip 28–32 of exon 2
 4* aactag27890/A319AT CAG327/T Skip 319–327 of exon 4
 8* ttttag40032/T533TG CAG553/A Skip 533–553 of exon 8
 9* ttatag41453/C610AT TAG626/T Skip 610–626 of exon 9

Data adapted from (26). Lowercase indicates intron sequences, uppercase indicates exon sequences, and/refers to an intron/exon boundary. Numbers in italic refer to cDNA numbering (base 1 is the A in the AUG initiation codon). All other numbers refer to genomic numbering (26).

*Indicates cryptic sites investigated in this study.