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Human (GRCh38.p14)
Description

barrier to autointegration nuclear assembly factor 1 [Source:HGNC Symbol;Acc:HGNC:17397]

Gene Synonyms

BAF

Location

Chromosome 11: 66,002,228-66,004,149 forward strand.

GRCh38:CM000673.2

About this gene

This gene has 8 transcripts (splice variants), 230 orthologues, 1 paralogue and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000312175.7BANF1-20173189aaENSP00000310275.2
 
Protein coding
CCDS8125O75531 NM_003860.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000533166.5BANF1-208113589aaENSP00000433760.1
 
Protein coding
CCDS8125O75531 -GENCODE BasicAPPRIS P1TSL:2
ENST00000445560.6BANF1-20294689aaENSP00000416128.2
 
Protein coding
CCDS8125O75531 -GENCODE BasicAPPRIS P1TSL:1
ENST00000527348.1BANF1-20567089aaENSP00000432867.1
 
Protein coding
CCDS8125O75531 -GENCODE BasicAPPRIS P1TSL:3
ENST00000530204.1BANF1-20758628aaENSP00000431785.1
 
Protein coding
E9PJJ8 -TSL:5CDS 3' incomplete
ENST00000524628.1BANF1-203612No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000528648.1BANF1-206362No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000524663.1BANF1-204251No protein-
 
Protein coding CDS not defined
--TSL:3