Human (GRCh38.p14)
Description

basal body orientation factor 1 [Source:HGNC Symbol;Acc:HGNC:19855]

Gene Synonyms

C14ORF45, CCDC176, FBB10

Location
About this transcript

This transcript has 12 exons, is annotated with 9 domains and features, is associated with 20186 variant alleles and maps to 443 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000394009.5BBOF1-2013113529aaENSP00000377577.3
 
Protein coding
CCDS32119Q8ND07 NM_025057.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000464394.5BBOF1-203689124aaENSP00000451659.1
 
Protein coding
G3V488 -TSL:3CDS 3' incomplete
ENST00000463558.3BBOF1-20255065aaENSP00000480689.1
 
Protein coding
A0A0B4J2D7 -GENCODE basicTSL:2
ENST00000492026.4BBOF1-2061715No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000489323.5BBOF1-205571No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000477986.2BBOF1-204703No protein-
 
Retained intron
--TSL:3
ENST00000492247.3BBOF1-207544No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 12, Coding exons: 12, Transcript length: 3,113 bps, Translation length: 529 residues

MANE

This MANE Select transcript contains ENSP00000377577 and matches to NM_025057.3 and NP_079333.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8ND07

CCDS

This transcript is a member of the Human CCDS set: CCDS32119

Transcript Support Level (TSL)

TSL:2

Version

ENST00000394009.5

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.

GENCODE basic gene

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