Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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ID History
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Gene: ENSRNOG00000034226

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Description

T cell leukemia/lymphoma 1B, 3 [Ensembl NN prediction with score 77.73%]

Location

Primary_assembly 8: 38,651,146-38,667,995 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000047211.3	-	312	103aa	ENSRNOP00000041911.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6TXI9	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,

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Summary

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