Human (GRCh38.p14)
Description

G-rich RNA sequence binding factor 1 [Source:HGNC Symbol;Acc:HGNC:4610]

Location
About this transcript

This transcript has 10 exons, is annotated with 15 domains and features, is associated with 9952 variant alleles and maps to 449 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000254799.11GRSF1-2016610480aaENSP00000254799.6
 
Protein coding
CCDS47069Q12849-1 NM_002092.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000499044.6GRSF1-2022491453aaENSP00000427354.1
 
Protein coding
H0YAK1 -TSL:2CDS 5' incomplete
ENST00000502323.5GRSF1-2031794318aaENSP00000425430.1
 
Protein coding
CCDS47070Q12849-5 -GENCODE basicTSL:5
ENST00000514161.5GRSF1-2071765417aaENSP00000421789.1
 
Protein coding
H0Y8R1 -TSL:2CDS 5' incomplete
ENST00000506453.1GRSF1-205925114aaENSP00000427644.1
 
Nonsense mediated decay
H0YAM1 -TSL:3CDS 5' incomplete
ENST00000508091.1GRSF1-206419No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000505068.5GRSF1-2043561No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 10, Coding exons: 8, Transcript length: 1,794 bps, Translation length: 318 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q12849

CCDS

This transcript is a member of the Human CCDS set: CCDS47070

Transcript Support Level (TSL)

TSL:5

Version

ENST00000502323.5

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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