Hi,

According to ucsc genome browser, NR_002891 maps to the following
genomic location. These two mappings show very different number exons.
One is 1, the other is 12.

I don't understand why a single transcript could come from two genomic
location that have very different intro/exon structures. Are these
mappings real? Or one of them is an artifact. Or the underlining
genome assembly (mm9) is defective at one of these locations?

NR_002891 at chr19:12979721-12981475
NR_002891 at chr10:5917375-5943370

--
Regards,
Peng
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