Human (GRCh38.p14)
Description

retinoic acid receptor gamma [Source:HGNC Symbol;Acc:HGNC:9866]

Gene Synonyms

NR1B3, RAR-GAMMA, RARC, RARGAMMA

Location
About this transcript

This transcript has 10 exons, is annotated with 52 domains and features, is associated with 10325 variant alleles and maps to 642 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000425354.7RARG-2032917454aaENSP00000388510.2
 
Protein coding
CCDS8850P13631-1 NM_000966.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT2TSL:1
ENST00000394426.5RARG-2022640382aaENSP00000377947.2
 
Protein coding
CCDS58236P13631-3 -GENCODE basicTSL:1
ENST00000338561.9RARG-2011836443aaENSP00000343698.5
 
Protein coding
CCDS41790P13631-2 -GENCODE basicAPPRIS P4TSL:1
ENST00000543726.1RARG-2041779432aaENSP00000444335.1
 
Protein coding
CCDS58237P13631-4 -GENCODE basicTSL:2
ENST00000550362.5RARG-21394415aaENSP00000454385.1
 
Protein coding
H3BMH6 -TSL:2CDS 3' incomplete
ENST00000551158.5RARG-21558632aaENSP00000454604.1
 
Protein coding
H3BMY6 -TSL:2CDS 3' incomplete
ENST00000546717.1RARG-20755557aaENSP00000454417.1
 
Protein coding
H3BMK1 -TSL:4CDS 3' incomplete
ENST00000543762.5RARG-2051620No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000550350.5RARG-212583No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000550721.5RARG-214576No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000546377.1RARG-206560No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000551501.5RARG-216555No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000549859.1RARG-210544No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000552901.1RARG-218523No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000550265.5RARG-2111549No protein-
 
Retained intron
--TSL:2
ENST00000548284.1RARG-208556No protein-
 
Retained intron
--TSL:1
ENST00000551580.1RARG-217554No protein-
 
Retained intron
--TSL:4
ENST00000548317.1RARG-209517No protein-
 
Retained intron
--TSL:2

Protein domains for ENSP00000388510.2