Description

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

Location
INSDC coordinates

chromosome:GRCh37:CM000670.1:30891317:31031285:1

Transcripts

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.--
Stable ID

ENSG00000165392.5

Status

Current

Latest Version

ENSG00000165392.5

Release: 75 (current)

Assembly: GRCh37

Database: homo_sapiens_core_75_37

Associated archived IDs for this stable ID version

No associated IDs found

Gene-based displays