Human (GRCh38.p14)
Description

retinoic acid receptor responder 1 [Source:HGNC Symbol;Acc:HGNC:9867]

Gene Synonyms

LXNL, TIG1

About this transcript

This transcript has 6 exons, is annotated with 21 domains and features, is associated with 15009 variant alleles and maps to 517 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000237696.10RARRES1-2011713294aaENSP00000237696.5
 
Protein coding
CCDS3184P49788-1 NM_206963.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P3TSL:1
ENST00000879325.1RARRES1-2062040290aaENSP00000549384.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT2
ENST00000950251.1RARRES1-2071967273aaENSP00000620310.1
 
Protein coding
--GENCODE Basic
ENST00000950252.1RARRES1-2081743279aaENSP00000620311.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000950253.1RARRES1-2091432273aaENSP00000620312.1
 
Protein coding
--GENCODE Basic
ENST00000479756.1RARRES1-204839228aaENSP00000418556.1
 
Protein coding
CCDS54665P49788-2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000498640.1RARRES1-205532No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000462663.5RARRES1-202366No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000471444.1RARRES1-203187No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 6, Coding exons: 6, Transcript length: 1,713 bps, Translation length: 294 residues

MANE

This MANE Select transcript contains ENSP00000237696 and matches to NM_206963.2 and NP_996846.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P49788

CCDS

This transcript is a member of the Human CCDS set: CCDS3184

Transcript Support Level (TSL)

TSL:1

Version

ENST00000237696.10

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.