Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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  - Gene tree
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Ontologies
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Gene: RAD52 ENSSSCG00000000754

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Description

RAD52 homolog, DNA repair protein [Source:VGNC Symbol;Acc:VGNC:92060]

Location

Primary_assembly 5: 68,143,646-68,169,670 reverse strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 2 transcripts (splice variants) and 198 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000042724.3	RAD52-202	2311	406aa	ENSSSCP00000044772.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UGK6 B0M1M7	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,
ENSSSCT00000000818.5	RAD52-201	1661	381aa	ENSSSCP00000000802.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A288CFZ6 A0A4X1UGJ7	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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