Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 7 exons, is annotated with 2 domains and features, is associated with 23079 variant alleles and maps to 451 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: 7, Coding exons: 7, Transcript length: 3,029 bps, Translation length: 351 residues

Transcript Support Level (TSL)

TSL:2

Version

ENST00000515604.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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