Human (GRCh38.p14)
Description

Ras association domain family member 1 [Source:HGNC Symbol;Acc:HGNC:9882]

Gene Synonyms

123F2, NORE2A, RDA32, REH3P21

Location

Chromosome 3: 50,329,782-50,340,980 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 10 transcripts (splice variants), 277 orthologues and 5 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000359365.9RASSF1-2031847340aaENSP00000352323.4
 
Protein coding
CCDS43096Q9NS23-2 NM_007182.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000357043.6RASSF1-2021864344aaENSP00000349547.2
 
Protein coding
CCDS2820Q9NS23-1 -GENCODE basicTSL:1
ENST00000616212.4RASSF1-2101842189aaENSP00000482696.1
 
Protein coding
CCDS2822Q9NS23-3 -GENCODE basicTSL:2
ENST00000327761.7RASSF1-2011757270aaENSP00000333327.3
 
Protein coding
CCDS2821Q9NS23-4 -GENCODE basicTSL:1
ENST00000395126.7RASSF1-2051657189aaENSP00000378558.3
 
Protein coding
CCDS2822Q9NS23-3 -GENCODE basicTSL:1
ENST00000395117.6RASSF1-204174592aaENSP00000378549.2
 
Nonsense mediated decay
Q9NS23-6 -TSL:2
ENST00000482447.1RASSF1-2071711152aaENSP00000433000.1
 
Nonsense mediated decay
Q9NS23-7 -TSL:1
ENST00000488024.1RASSF1-2081385No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000478619.1RASSF1-2062060No protein-
 
Retained intron
--TSL:2
ENST00000494145.1RASSF1-2091358No protein-
 
Retained intron
--TSL:1