Human (GRCh38.p14)
Description

INS-IGF2 readthrough [Source:HGNC Symbol;Acc:HGNC:33527]

Location
About this transcript

This transcript has 7 exons, is annotated with 6 domains and features, is associated with 15327 variant alleles and maps to 689 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000397270.1INS-IGF2-202828200aaENSP00000380440.1
 
Protein coding
F8WCM5-1 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000356578.8INS-IGF2-2011706200aaENSP00000348986.4
 
Nonsense mediated decay
F8WCM5-1 -TSL:5
Statistics

Exons: 7, Coding exons: 3, Transcript length: 1,706 bps, Translation length: 200 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: F8WCM5

Transcript Support Level (TSL)

TSL:5

Version

ENST00000356578.8

Type

Nonsense mediated decay

Annotation Method

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