Human (GRCh38.p14)
Description

C1QTNF3-AMACR readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:49198]

Location
About this transcript

This transcript has 9 exons, is annotated with 1 domain and feature, is associated with 53690 variant alleles and maps to 875 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000382079.3C1QTNF3-AMACR-2013424284aaENSP00000371511.3
 
Nonsense mediated decay
E9PGA6 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:2
Statistics

Exons: 9, Coding exons: 8, Transcript length: 3,424 bps, Translation length: 284 residues

Transcript Support Level (TSL)

TSL:2

Version

ENST00000382079.3

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.

GENCODE primary gene

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