Human (GRCh38.p14)
Description

CCL15-CCL14 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:44436]

Location
About this transcript

This transcript has 7 exons, is annotated with 1 domain and feature, is associated with 7392 variant alleles and maps to 468 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000616694.1CCL15-CCL14-202999113aaENSP00000481402.1
 
Nonsense mediated decay
CCDS11304A0A0B4J2E2 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000610751.4CCL15-CCL14-201977113aaENSP00000481940.1
 
Nonsense mediated decay
CCDS11304A0A0B4J2E2 -APPRIS P1TSL:2
Statistics

Exons: 7, Coding exons: 4, Transcript length: 999 bps, Translation length: 113 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS11304

Transcript Support Level (TSL)

TSL:2

Version

ENST00000616694.1

Type

Nonsense mediated decay

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.