Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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ID History
- Gene history

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Gene: AABR07017236.2 ENSRNOG00000057837

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Location

Primary_assembly 15: 19,580,339-19,641,140 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 5 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSRNOT00000126009.1	AABR07017236.2-202	1897	No protein	-	lncRNA	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,
ENSRNOT00000149269.1	AABR07017236.2-205	1825	No protein	-	lncRNA	-
ENSRNOT00000130673.1	AABR07017236.2-204	1706	No protein	-	lncRNA	-
ENSRNOT00000128633.1	AABR07017236.2-203	1560	No protein	-	lncRNA	-
ENSRNOT00000092092.3	AABR07017236.2-201	1175	No protein	-	lncRNA	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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