Human (GRCh38.p14)
Description

FAM47E-STBD1 readthrough [Source:HGNC Symbol;Acc:HGNC:44667]

Location
About this transcript

This transcript has 3 exons, is annotated with 1 domain and feature, is associated with 22806 variant alleles and maps to 292 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000515604.5FAM47E-STBD1-2043029351aaENSP00000422067.1
 
Protein coding
--Ensembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000514140.1FAM47E-STBD1-2022532191aaENSP00000423044.2
 
Protein coding
D6RA91 -TSL:2CDS 5' incomplete
ENST00000651133.1FAM47E-STBD1-205238853aaENSP00000498232.1
 
Nonsense mediated decay
F6W5V1 --
ENST00000509377.1FAM47E-STBD1-201148453aaENSP00000425528.2
 
Nonsense mediated decay
F6W5V1 -TSL:2
ENST00000514365.5FAM47E-STBD1-203146553aaENSP00000424458.1
 
Nonsense mediated decay
F6W5V1 -TSL:2
Statistics

Exons: 3, Coding exons: 2, Transcript length: 1,465 bps, Translation length: 53 residues

Transcript Support Level (TSL)

TSL:2

Version

ENST00000514365.5

Type

Nonsense mediated decay

Annotation Method

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