Human (GRCh38.p14)
Description

Ras association domain family member 3 [Source:HGNC Symbol;Acc:HGNC:14271]

Location

Chromosome 12: 64,507,001-64,697,564 forward strand.

GRCh38:CM000674.2

About this gene

This gene has 5 transcripts (splice variants), 215 orthologues and 5 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000542104.6RASSF3-2033507238aaENSP00000443021.1
 
Protein coding
CCDS8969Q86WH2-1 NM_178169.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000637125.1RASSF3-2051060299aaENSP00000490100.1
 
Protein coding
A0A1B0GUG6 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000636333.1RASSF3-20419264aaENSP00000490955.1
 
Protein coding
A0A1B0GWJ9 -TSL:5CDS 3' incomplete
ENST00000283172.8RASSF3-201109990aaENSP00000283172.4
 
Nonsense mediated decay
Q86WH2-2 -TSL:2
ENST00000540088.1RASSF3-202435No protein-
 
Protein coding CDS not defined
--TSL:5