Human (GRCh38.p14)
Description

forkhead box N4 [Source:HGNC Symbol;Acc:HGNC:21399]

About this transcript

This transcript has 10 exons, is annotated with 18 domains and features, is associated with 13763 variant alleles and maps to 499 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000299162.10FOXN4-2013416517aaENSP00000299162.5
 
Protein coding
CCDS9126Q96NZ1-1 NM_213596.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000355216.5FOXN4-2022958337aaENSP00000347354.1
 
Protein coding
Q96NZ1-3 -GENCODE basicTSL:2
ENST00000468516.1FOXN4-204159384aaENSP00000474754.1
 
Protein coding
S4R3U5 -TSL:2CDS 5' incomplete
ENST00000423960.1FOXN4-2031219218aaENSP00000408085.1
 
Nonsense mediated decay
A0A0C4DG65 -TSL:1CDS 5' incomplete
Statistics

Exons: 10, Coding exons: 9, Transcript length: 3,416 bps, Translation length: 517 residues

MANE

This MANE Select transcript contains ENSP00000299162 and matches to NM_213596.3 and NP_998761.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96NZ1

CCDS

This transcript is a member of the Human CCDS set: CCDS9126

Transcript Support Level (TSL)

TSL:1

Version

ENST00000299162.10

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.