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 13 exons, is annotated with 6 domains and features, is associated with 15916 variant alleles and maps to 558 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: 13, Coding exons: 13, Transcript length: 4,711 bps, Translation length: 622 residues

MANE

This MANE Select transcript contains ENSP00000197268 and matches to NM_020853.2 and NP_065904.1

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:1

Version

ENST00000197268.13

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.