Human (GRCh38.p14)
Description

WD repeat domain 89 [Source:HGNC Symbol;Acc:HGNC:20489]

Gene Synonyms

C14ORF150, MGC9907

Location
About this transcript

This transcript has 3 exons, is annotated with 17 domains and features, is associated with 21226 variant alleles and maps to 442 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000620954.2WDR89-2043109387aaENSP00000480112.1
 
Protein coding
CCDS9759A0A024R667 Q96FK6 NM_080666.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:NA
ENST00000394942.2WDR89-2022993387aaENSP00000378399.2
 
Protein coding
CCDS9759A0A024R667 Q96FK6 -GENCODE basicAPPRIS P1TSL:5
ENST00000267522.7WDR89-2011687387aaENSP00000267522.3
 
Protein coding
CCDS9759A0A024R667 Q96FK6 -GENCODE basicAPPRIS P1TSL:1
ENST00000554717.1WDR89-203976226aaENSP00000451702.1
 
Protein coding
G3V4B8 -TSL:2CDS 3' incomplete
Statistics

Exons: 3, Coding exons: 1, Transcript length: 3,109 bps, Translation length: 387 residues

MANE

This MANE Select transcript contains ENSP00000480112 and matches to NM_080666.4 and NP_542397.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96FK6

CCDS

This transcript is a member of the Human CCDS set: CCDS9759

Transcript Support Level (TSL)

TSL:NA

Version

ENST00000620954.2

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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