Data for: A survey of transcripts generated by spinal muscular atrophy genes

Description

Annotated sequence of the SMN1 locus. The genomic sequence of SMN1 and 10,000 bases upstream and downstream are given. Sequence composition and numbering are derived from the GRCh38 version of the human genome. Common exons of SMN are highlighted in light blue, rare exons are highlighted in pink. Underlined bases indicate sequences of interest; labels are provided above underlined bases. Start codons, stop codons, and non-canonical splice sites are marked in red. Bold, purple sequences indicate location of SMN-AS1 antisense transcript. Abbreviations: Cnt., continued; uORF, upstream open reading frame; ISS-N1, intronic splicing silencer N1

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