Human (GRCh38.p14)
Description

WD repeat domain 55 [Source:HGNC Symbol;Acc:HGNC:25971]

Gene Synonyms

FLJ20195, FLJ21702

About this transcript

This transcript has 7 exons, is annotated with 21 domains and features, is associated with 3554 variant alleles and maps to 653 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000358337.10WDR55-2013852383aaENSP00000351100.5
 
Protein coding
CCDS4235Q9H6Y2-1 NM_017706.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000504897.2WDR55-2022953222aaENSP00000439719.1
 
Nonsense mediated decay
G3V1J0 -TSL:2
ENST00000506393.5WDR55-2032477137aaENSP00000426304.1
 
Nonsense mediated decay
D6RGJ8 -TSL:2
ENST00000520764.1WDR55-2051696No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000511232.5WDR55-2043812No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 3,852 bps, Translation length: 383 residues

MANE

This MANE Select transcript contains ENSP00000351100 and matches to NM_017706.5 and NP_060176.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9H6Y2

CCDS

This transcript is a member of the Human CCDS set: CCDS4235

Transcript Support Level (TSL)

TSL:1

Version

ENST00000358337.10

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.