Human (GRCh38.p14)
Description

IFNAR2-IL10RB readthrough [Source:NCBI gene (formerly Entrezgene);Acc:127882475]

Location
About this transcript

This transcript has 15 exons, is annotated with 1 domain and feature, is associated with 30248 variant alleles and maps to 903 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000433395.7IFNAR2-IL10RB-2022112545aaENSP00000388223.3
 
Protein coding
H0Y3Z8 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000683116.1IFNAR2-IL10RB-2053943515aaENSP00000508125.1
 
Nonsense mediated decay
CCDS13621---
ENST00000646150.1IFNAR2-IL10RB-2033770515aaENSP00000496248.1
 
Nonsense mediated decay
CCDS13621---
ENST00000682009.1IFNAR2-IL10RB-2042941237aaENSP00000506919.1
 
Nonsense mediated decay
A0A804HI63 --
ENST00000432231.1IFNAR2-IL10RB-201753112aaENSP00000413946.1
 
Nonsense mediated decay
H7C3V1 -TSL:2CDS 5' incomplete
Statistics

Exons: 15, Coding exons: 8, Transcript length: 3,770 bps, Translation length: 515 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS13621

Version

ENST00000646150.1

Type

Nonsense mediated decay

Annotation Method

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

Annotation Attributes

RNA-Seq supported only [Definitions]