Human (GRCh38.p14)
Description

RTEL1-TNFRSF6B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44095]

Location
About this transcript

This transcript has 35 exons, is annotated with 1 domain and feature, is associated with 27270 variant alleles and maps to 1645 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000492259.6RTEL1-TNFRSF6B-2024824785aaENSP00000457428.1
 
Nonsense mediated decay
D6RA96 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000697815.1RTEL1-TNFRSF6B-2043597No protein-
 
Protein coding CDS not defined
---
ENST00000496281.2RTEL1-TNFRSF6B-2035843No protein-
 
Retained intron
--TSL:2
ENST00000480273.5RTEL1-TNFRSF6B-2015751No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 35, Coding exons: 23, Transcript length: 4,824 bps, Translation length: 785 residues

Transcript Support Level (TSL)

TSL:5

Version

ENST00000492259.6

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.