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Transcript: ENST00000416089.1 ARHGAP42P2-201

Description

ARHGAP42 pseudogene 2 [Source:HGNC Symbol;Acc:HGNC:43939]

Location

About this transcript

This transcript has 8 exons, is associated with 1253 variant alleles and maps to 204 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000416089.1	ARHGAP42P2-201	2140	No protein	-	Pseudogene that can contain introns since produced by gene duplication.Unprocessed pseudogene		-	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL NA: A transcript that was not analysed for TSL. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:NA,

Summary

Statistics

Exons: 8, Coding exons: 0, Transcript length: 2,140 bps,

Transcript Support Level (TSL)

TSL:NA

Version

ENST00000416089.1

Type

Unprocessed pseudogene

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.