Human (GRCh38.p14)
Description

regulator of G protein signaling 14 [Source:HGNC Symbol;Acc:HGNC:9996]

About this transcript

This transcript has 15 exons, is annotated with 44 domains and features, is associated with 7360 variant alleles and maps to 731 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000408923.8RGS14-2012323566aaENSP00000386229.3
 
Protein coding
CCDS43405O43566-7 NM_006480.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000511890.1RGS14-2091536437aaENSP00000422329.1
 
Protein coding
H0Y8W3 -TSL:1CDS 5' incomplete
ENST00000506944.1RGS14-207590No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000503110.5RGS14-205587No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000425155.6RGS14-2022329No protein-
 
Retained intron
--TSL:2
ENST00000514102.5RGS14-212875No protein-
 
Retained intron
--TSL:2
ENST00000514713.5RGS14-213817No protein-
 
Retained intron
--TSL:1
ENST00000504631.5RGS14-206661No protein-
 
Retained intron
--TSL:3
ENST00000512490.1RGS14-211565No protein-
 
Retained intron
--TSL:2
ENST00000512000.1RGS14-210559No protein-
 
Retained intron
--TSL:3
ENST00000502731.5RGS14-203472No protein-
 
Retained intron
--TSL:2
ENST00000503044.5RGS14-204458No protein-
 
Retained intron
--TSL:2
ENST00000509289.1RGS14-208414No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 15, Coding exons: 15, Transcript length: 2,323 bps, Translation length: 566 residues

MANE

This MANE Select transcript contains ENSP00000386229 and matches to NM_006480.5 and NP_006471.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: O43566

CCDS

This transcript is a member of the Human CCDS set: CCDS43405

Transcript Support Level (TSL)

TSL:1

Version

ENST00000408923.8

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.