Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: CHRNA7 ENSPTRG00000006865

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Description

cholinergic receptor nicotinic alpha 7 subunit [Source:VGNC Symbol;Acc:VGNC:108899]

Location

Chromosome 15: 12,270,932-12,422,705 forward strand.

Pan_tro_3.0:CM000329.3

About this gene

This gene has 2 transcripts (splice variants), 243 orthologues and 49 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000012669.3	CHRNA7-201	6191	511aa	ENSPTRP00000011728.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2Q930	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
ENSPTRT00000081260.1	CHRNA7-202	957	319aa	ENSPTRP00000066996.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RQN7 A0A6D2WLE8	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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Summary

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