Transcript: ENSDART00000074746.3 smcr8a-201

Description

Smith-Magenis syndrome chromosome region, candidate 8a [Source:NCBI gene;Acc:558696]

Location

About this transcript

This transcript has 2 exons, is annotated with 11 domains and features, is associated with 267 variant alleles and maps to 143 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000074746.3	smcr8a-201	2605	853aa	ENSDARP00000069232.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FA21	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 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,

Summary

Statistics

Exons: 2, Coding exons: 2, Transcript length: 2,605 bps, Translation length: 853 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: E7FA21

Version

ENSDART00000074746.3

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.