Transcript: ENSSSCT00000054990.2 TLX1-201

Description

T cell leukemia homeobox 1 [Source:HGNC Symbol;Acc:HGNC:5056]

Location

About this transcript

This transcript has 4 exons, is annotated with 20 domains and features and is associated with 280 variant alleles.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000054990.2	TLX1-201	2355	334aa	ENSSSCP00000055444.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BGH2	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: 4, Coding exons: 4, Transcript length: 2,355 bps, Translation length: 334 residues

Version

ENSSSCT00000054990.2

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

Frameshift introns

Frameshift introns occur at intron number(s) 1.