Description

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

Synonyms

RECQ3, RECQL2

Location
About this transcript

This transcript has 35 exons, is annotated with 31 domains and features, is associated with 551 variations and maps to 59 oligo probes.

Gene
NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
WRN-001ENST0000029813952151432aaENSP00000298139
 
Protein coding
CCDS6082Q14191 NM_000553
NP_000544
TSL:1GENCODE basicAPPRIS P1
WRN-002ENST000005216203593No protein-
 
Retained intron
---TSL:1
WRN-003ENST00000520169629No protein-
 
Retained intron
---TSL:3
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

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14191

Transcript Support Level (TSL)

TSL:1

Ensembl version

ENST00000298139.5

Type

Known protein coding

Annotation 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:

Havana transcript:
GENCODE basic gene

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

Transcript-based displays