Human (GRCh37.p13)
Description

centrosomal protein 89kDa [Source:HGNC Symbol;Acc:25907]

Gene Synonyms

CCDC123, CEP123, FLJ14640

Location
About this transcript

This transcript has 19 exons, is annotated with 15 domains and features, is associated with 39122 variant alleles and maps to 742 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000305768.5CEP89-0012607783aaENSP00000306105.4
 
Protein coding
CCDS32987Q96ST8 NM_032816.3GENCODE basic
ENST00000590597.2CEP89-0051340356aaENSP00000466442.1
 
Protein coding
Q96ST8 -GENCODE basic
ENST00000593276.2CEP89-006682217aaENSP00000467839.1
 
Protein coding
--CDS 5' incomplete
ENST00000586984.2CEP89-0042482428aaENSP00000465141.1
 
Nonsense mediated decay
K7EJF0 --
ENST00000591698.1CEP89-0022367173aaENSP00000467544.1
 
Nonsense mediated decay
K7EPU8 -CDS 5' incomplete
ENST00000591863.1CEP89-0102903No protein-
 
Processed transcript
---
ENST00000592401.1CEP89-008558No protein-
 
Processed transcript
---
ENST00000591205.1CEP89-007596No protein-
 
Retained intron
---
Statistics

Exons: 19, Coding exons: 19, Transcript length: 2,607 bps, Translation length: 783 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96ST8

CCDS

This transcript is a member of the Human CCDS set: CCDS32987

Version

ENST00000305768.5

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.

Stop codons

This transcript has a variant, rs745961, that causes a stop codon to be lost in at least 10% of HapMap or 1000 Genome population(s) CSHL-HAPMAP:HapMap-CEU, CSHL-HAPMAP:HAPMAP-GIH, CSHL-HAPMAP:HAPMAP-TSI, ESP6500:African_American, ESP6500:European_American.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000451300 (version 2)
GENCODE basic gene

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