Transcript: ENSRNOT00000001894.7 Pcolce-201

Description

procollagen C-endopeptidase enhancer [Source:RGD Symbol;Acc:3270]

Gene Synonyms

MGC105446, PCPE, PCPE-1

Location

About this transcript

This transcript has 8 exons, is annotated with 30 domains and features, is associated with 90 variant alleles and maps to 157 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000080775.3	Pcolce-202	1636	493aa	ENSRNOP00000073700.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5RJN2	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,
ENSRNOT00000001894.7	Pcolce-201	1725	487aa	ENSRNOP00000001887.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2PZS7	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,

Summary

Statistics

Exons: 8, Coding exons: 8, Transcript length: 1,725 bps, Translation length: 487 residues

Version

ENSRNOT00000001894.7

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.