Human (GRCh38.p14)
Description

neuromedin U [Source:HGNC Symbol;Acc:HGNC:7859]

Location
About this transcript

This transcript has 9 exons, is annotated with 9 domains and features, is associated with 17583 variant alleles and maps to 310 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264218.7NMU-201816174aaENSP00000264218.3
 
Protein coding
CCDS3501A0A250SH36 P48645 NM_006681.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000511469.5NMU-205756158aaENSP00000422399.1
 
Protein coding
CCDS75125A0A0B4J202 -GENCODE basicTSL:3
ENST00000505262.5NMU-202693147aaENSP00000424246.1
 
Protein coding
D6RBC9 -GENCODE basicTSL:3
ENST00000507338.1NMU-203658149aaENSP00000422870.1
 
Protein coding
CCDS77914E9PDJ7 -GENCODE basicTSL:3
ENST00000515325.5NMU-206616No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000509371.1NMU-204283No protein-
 
Protein coding CDS not defined
--TSL:1
Statistics

Exons: 9, Coding exons: 8, Transcript length: 658 bps, Translation length: 149 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS77914

Transcript Support Level (TSL)

TSL:3

Version

ENST00000507338.1

Type

Protein coding

Annotation Method

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

GENCODE basic gene

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