Human (GRCh38.p14)
Description

Ras association domain family member 4 [Source:HGNC Symbol;Acc:HGNC:20793]

Gene Synonyms

AD037, MGC44914

Location

Chromosome 10: 44,959,407-44,995,891 forward strand.

GRCh38:CM000672.2

About this gene

This gene has 12 transcripts (splice variants), 171 orthologues and 5 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000340258.10RASSF4-2013631321aaENSP00000339692.4
 
Protein coding
CCDS7208Q9H2L5-1 NM_032023.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000427758.5RASSF4-202528151aaENSP00000409767.1
 
Protein coding
Q5T739 -TSL:3CDS 3' incomplete
ENST00000484477.2RASSF4-21049184aaENSP00000476848.1
 
Protein coding
V9GYK1 -TSL:2CDS 5' incomplete
ENST00000428466.1RASSF4-203435123aaENSP00000413468.1
 
Protein coding
Q5T737 -TSL:3CDS 5' incomplete
ENST00000483709.6RASSF4-20973449aaENSP00000473555.1
 
Nonsense mediated decay
R4GNA4 -TSL:5
ENST00000472561.5RASSF4-208892No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000471808.1RASSF4-206410No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000462822.1RASSF4-204354No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000489171.5RASSF4-2114350No protein-
 
Retained intron
--TSL:1
ENST00000471941.5RASSF4-2072275No protein-
 
Retained intron
--TSL:2
ENST00000465735.5RASSF4-2052207No protein-
 
Retained intron
--TSL:2
ENST00000493490.1RASSF4-212479No protein-
 
Retained intron
--TSL:2