Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: RNASEH2A ENSSSCG00000013737

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Description

ribonuclease H2 subunit A [Source:VGNC Symbol;Acc:VGNC:92338]

Location

Primary_assembly 2: 66,193,197-66,207,697 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 2 transcripts (splice variants) and 185 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000054730.3	RNASEH2A-202	2618	327aa	ENSSSCP00000041485.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AC66 A0A8D1UHM5	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,
ENSSSCT00000015011.5	RNASEH2A-201	1173	301aa	ENSSSCP00000014606.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1A232 F1SDX8	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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