Human (GRCh38.p14)
Description

FA core complex associated protein 24 [Source:HGNC Symbol;Acc:HGNC:28467]

Gene Synonyms

C19ORF40, FLJ46828, MGC32020

Location

Chromosome 19: 32,972,209-32,978,229 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 9 transcripts (splice variants) and 209 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000588258.6FAAP24-2022313215aaENSP00000466121.1
 
Protein coding
CCDS12426A0A0S2Z5V6 Q9BTP7 NM_152266.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000699960.1FAAP24-2081245215aaENSP00000514718.1
 
Protein coding
CCDS12426A0A0S2Z5V6 Q9BTP7 -GENCODE basicAPPRIS P1
ENST00000590281.1FAAP24-205865215aaENSP00000468475.1
 
Protein coding
CCDS12426A0A0S2Z5V6 Q9BTP7 -GENCODE basicAPPRIS P1TSL:3
ENST00000589646.5FAAP24-203836120aaENSP00000465569.1
 
Protein coding
CCDS74327K7EKQ4 -GENCODE basicTSL:3
ENST00000590179.1FAAP24-204784120aaENSP00000465728.1
 
Protein coding
CCDS74327K7EKQ4 -GENCODE basicTSL:2
ENST00000254262.9FAAP24-20187569aaENSP00000254262.5
 
Nonsense mediated decay
X6R368 -TSL:2
ENST00000591791.1FAAP24-206768No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000699961.1FAAP24-2091956No protein-
 
Retained intron
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ENST00000699959.1FAAP24-2071266No protein-
 
Retained intron
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