Human (GRCh38.p14)
Description

FA core complex associated protein 100 [Source:HGNC Symbol;Acc:HGNC:26171]

Gene Synonyms

C17ORF70, FLJ22175

Location

Chromosome 17: 81,539,885-81,553,961 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 7 transcripts (splice variants) and 189 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000327787.13FAAP100-2013597881aaENSP00000333283.8
 
Protein coding
CCDS32765Q0VG06-1 NM_025161.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000425898.2FAAP100-2022996530aaENSP00000399674.2
 
Protein coding
E7EVV8 -GENCODE basicTSL:1
ENST00000541246.1FAAP100-2051101300aaENSP00000438149.1
 
Protein coding
F5H095 -TSL:5CDS 3' incomplete
ENST00000544302.1FAAP100-2061091249aaENSP00000444241.1
 
Protein coding
F5GZS4 -TSL:2CDS 3' incomplete
ENST00000536161.1FAAP100-204924172aaENSP00000443415.1
 
Protein coding
F5H5G6 -TSL:3CDS 3' incomplete
ENST00000443656.6FAAP100-203382297aaENSP00000395348.2
 
Nonsense mediated decay
J3KQD8 -TSL:1
ENST00000545865.1FAAP100-207689110aaENSP00000459776.1
 
Nonsense mediated decay
I3L2L9 -TSL:2CDS 5' incomplete