Transcript: ENSRNOT00000008030.9 Nsg1-201

Description

neuronal vesicle trafficking associated 1 [Source:RGD Symbol;Acc:2222]

Gene Synonyms

Bsmrb, Neep21, PEP1

Location

About this transcript

This transcript has 3 exons, is annotated with 8 domains and features, is associated with 94 variant alleles and maps to 140 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000118922.2	Nsg1-202	2513	185aa	ENSRNOP00000097258.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IJU5 P02683	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,
ENSRNOT00000008030.9	Nsg1-201	1987	146aa	ENSRNOP00000008030.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACR3 A0A8L2Q3K9	APPRIS ALT1: 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 is conserved in at least 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 ALT1,

Summary

Statistics

Exons: 3, Coding exons: 3, Transcript length: 1,987 bps, Translation length: 146 residues

Version

ENSRNOT00000008030.9

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.