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Human (GRCh38.p14)
Description

regulatory factor X associated protein [Source:HGNC Symbol;Acc:HGNC:9988]

Location

Chromosome 13: 36,819,222-36,829,104 forward strand.

GRCh38:CM000675.2

About this gene

This gene has 2 transcripts (splice variants), 189 orthologues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000255476.3RFXAP-2012306272aaENSP00000255476.3
 
Protein coding
CCDS9359O00287 NM_000538.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000472888.1RFXAP-202534No protein-
 
Protein coding CDS not defined
--TSL:3