Summary
- Splice variants
- Transcript comparison
- Gene alleles
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Comparative Genomics
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Gene: CG42326 FBgn0259226

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Gene Synonyms

CG42326

Location

Primary_assembly 2R: 8,573,368-8,584,779 reverse strand.

BDGP6.46:AE013599.5

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0339346	CG42326-RE	5244	1376aa	FBpp0308444	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0B4LEX9 A1Z7G1	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
FBtr0299788	CG42326-RD	3400	952aa	FBpp0289066	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1Z7G0 B6IDK6 Q86P35	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,

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Summary

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