Human (GRCh38.p14)
Description

nucleolar protein 4 like [Source:HGNC Symbol;Acc:HGNC:16106]

Gene Synonyms

C20ORF112, C20ORF113, DJ1184F4.2, DJ1184F4.4, DKFZP566G1424

Location
About this transcript

This transcript has 11 exons, is annotated with 14 domains and features, is associated with 64189 variant alleles and maps to 674 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000621426.7NOL4L-2107023680aaENSP00000483523.1
 
Protein coding
CCDS74718A0A087X0N3 NM_001256798.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000359676.9NOL4L-2035991436aaENSP00000352704.5
 
Protein coding
CCDS13202Q96MY1-1 -GENCODE basicTSL:2
ENST00000375678.7NOL4L-2052042155aaENSP00000364830.3
 
Protein coding
Q5JYC0 -GENCODE basicTSL:2
ENST00000201961.6NOL4L-201971249aaENSP00000201961.3
 
Protein coding
Q5W149 -TSL:3CDS 5' incomplete
ENST00000326071.8NOL4L-20270191aaENSP00000317413.4
 
Protein coding
Q5JYB6 -GENCODE basicTSL:1
ENST00000375677.5NOL4L-204541123aaENSP00000364829.2
 
Protein coding
Q5JYC2 -TSL:3CDS 5' incomplete
ENST00000419612.1NOL4L-20631176aaENSP00000410774.1
 
Protein coding
H0Y778 -TSL:3CDS 5' incomplete
ENST00000475781.1NOL4L-2081127172aaENSP00000492149.1
 
Nonsense mediated decay
A0A1W2PQU1 -TSL:5
ENST00000485364.1NOL4L-209885No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000470428.1NOL4L-207307No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 11, Coding exons: 11, Transcript length: 7,023 bps, Translation length: 680 residues

MANE

This MANE Select transcript contains ENSP00000483523 and matches to NM_001256798.2 and NP_001243727.1

CCDS

This transcript is a member of the Human CCDS set: CCDS74718

Transcript Support Level (TSL)

TSL:5

Version

ENST00000621426.7

Type

Protein coding

Annotation Method

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

Annotation Attributes

not organism-supported [Definitions]

GENCODE basic gene

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