Summary
- Splice variants
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Gene: T24E12.6 WBGene00020775

Description

Uncharacterized protein [Source:NCBI gene;Acc:188864]

Location

WBcel235:BX284602.5

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
-	T24E12.6b.1	996	331aa	T24E12.6b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A9D7R4	-	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 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,
-	T24E12.6a.1	872	112aa	T24E12.6a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O44878	-	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,

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