Description

Werner syndrome, RecQ helicase-like [Source:HGNC Symbol;Acc:12791]

Location
Gene

This transcript is a product of gene ENSG00000165392

This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDSGENCODE basic
WRN-001ENST000002981395215ENSP000002981391432Protein codingGenes and/or transcript that contains an open reading frame (ORF).CCDS6082YThe GENCODE Basic set includes all genes in the GENCODE gene set but only a subset of the transcripts.
WRN-002ENST000005216203593No protein product-Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.--
WRN-003ENST00000520169629No protein product-Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.--
Statistics

Exons: 35 Coding exons: 34 Transcript length: 5,215 bps Translation length: 1,432 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS6082

Ensembl version

ENST00000298139.5

Type

Known protein coding

Prediction Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000376248 (version 1)
GENCODE basic gene

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

Transcript-based displays