Summary
Sequence
Protein Information
- Protein summary
- Domains & features
- Variants
- PDB 3D protein model
- AlphaFold predicted model
Genetic Variation
- Variant table
- Variant image
- Population comparison
- Comparison image
External References
- General identifiers
- Oligo probes
Supporting evidence
ID History
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Transcript: F18C5.2.1

Description

putative Werner syndrome ATP-dependent helicase homolog 1 [Source:NCBI gene;Acc:174081]

Location

About this transcript

This transcript has 16 exons, is annotated with 31 domains and features and maps to 62 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
F18C5.2.1	-	3287	1056aa	F18C5.2.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q19546	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: 16, Coding exons: 16, Transcript length: 3,287 bps, Translation length: 1,056 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q19546

Version

F18C5.2.1

Type

Protein coding

Annotation Method

Protein-coding model imported from WormBase