Human (GRCh38.p14)
Description

RAB4B-EGLN2 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44465]

Gene Synonyms

RERT-LNCRNA

Location
About this transcript

This transcript has 12 exons, is associated with 15794 variant alleles and maps to 753 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000594136.2RAB4B-EGLN2-2012774213aaENSP00000469872.1
 
Nonsense mediated decay
CCDS33030A0A024R0K8 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000601949.5RAB4B-EGLN2-203482No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000596216.2RAB4B-EGLN2-202932No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 12, Coding exons: 7, Transcript length: 2,774 bps, Translation length: 213 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS33030

Transcript Support Level (TSL)

TSL:2

Version

ENST00000594136.2

Type

Nonsense mediated decay

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.