Human (GRCh38.p14)
Description

forkhead box L3 [Source:HGNC Symbol;Acc:HGNC:54201]

Location
About this transcript

This transcript has 3 exons, is annotated with 14 domains and features, is associated with 994 variant alleles and maps to 115 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000506382.2FOXL3-201702233aaENSP00000492766.1
 
Protein coding
CCDS94042A0A1W2PRP0 NM_001374838.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000510017.1FOXL3-20253048aaENSP00000492517.1
 
Nonsense mediated decay
A0A1W2PRW6 -TSL:2CDS 5' incomplete
Statistics

Exons: 3, Coding exons: 3, Transcript length: 702 bps, Translation length: 233 residues

MANE

This MANE Select transcript contains ENSP00000492766 and matches to NM_001374838.1 and NP_001361767.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A0A1W2PRP0

CCDS

This transcript is a member of the Human CCDS set: CCDS94042

Transcript Support Level (TSL)

TSL:5

Version

ENST00000506382.2

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.