Human (GRCh38.p14)
Description

family with sequence similarity 234 member B [Source:HGNC Symbol;Acc:HGNC:29288]

Gene Synonyms

KIAA1467

Location
About this transcript

This transcript has 14 exons, is annotated with 1 domain and feature, is associated with 15916 variant alleles and maps to 397 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000197268.13FAM234B-2014711622aaENSP00000197268.8
 
Protein coding
CCDS31750A2RU67 NM_020853.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000537625.1FAM234B-2042011324aaENSP00000437974.1
 
Protein coding
Q69YM1 -TSL:1CDS 5' incomplete
ENST00000416494.6FAM234B-2022623622aaENSP00000394063.2
 
Nonsense mediated decay
CCDS31750A2RU67 -TSL:2
ENST00000535974.1FAM234B-203578No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000541950.1FAM234B-2061586No protein-
 
Retained intron
--TSL:2
ENST00000540455.1FAM234B-205539No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 14, Coding exons: 13, Transcript length: 2,623 bps, Translation length: 622 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: A2RU67

CCDS

This transcript is a member of the Human CCDS set: CCDS31750

Transcript Support Level (TSL)

TSL:2

Version

ENST00000416494.6

Type

Nonsense mediated decay

Annotation Method

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