Human (GRCh38.p14)
Description

WRN RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:12791]

Gene Synonyms

RECQ3, RECQL2

Location
About this transcript

This transcript has 35 exons, is annotated with 50 domains and features, is associated with 60719 variant alleles and maps to 916 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000298139.7WRN-20175751432aaENSP00000298139.5
 
Protein coding
CCDS6082Q14191 NM_000553.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000651642.1WRN-205627209aaENSP00000498779.1
 
Protein coding
A0A494C0Y6 -CDS 5' and 3' incomplete
ENST00000650667.1WRN-204505179aaENSP00000498593.1
 
Nonsense mediated decay
A0A494C0M3 --
ENST00000651946.1WRN-206772No protein-
 
Protein coding CDS not defined
---
ENST00000521620.5WRN-2033593No protein-
 
Retained intron
--TSL:1
ENST00000520169.1WRN-202629No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 35, Coding exons: 34, Transcript length: 7,575 bps, Translation length: 1,432 residues

MANE

This MANE Select transcript contains ENSP00000298139 and matches to NM_000553.6 and NP_000544.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14191

CCDS

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

Transcript Support Level (TSL)

TSL:1

Version

ENST00000298139.7

Type

Protein coding

Annotation Method

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

GENCODE basic gene

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