Human (GRCh38.p14)
Description

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

Location

Chromosome 4: 76,251,721-76,311,129 forward strand.

GRCh38:CM000666.2

About this gene

This gene has 5 transcripts (splice variants).

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