Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 13 exons, is annotated with 25 domains and features, is associated with 29885 variant alleles and maps to 602 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000433395.7IFNAR2-IL10RB-2022112545aaENSP00000388223.3
 
Protein coding
H0Y3Z8 -Ensembl CanonicalGENCODE PrimaryGENCODE 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: 13, Coding exons: 12, Transcript length: 2,112 bps, Translation length: 545 residues

Transcript Support Level (TSL)

TSL:5

Version

ENST00000433395.7

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.

GENCODE primary gene

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