Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 5 exons, is annotated with 20 domains and features, is associated with 7315 variant alleles and maps to 305 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: 5, Coding exons: 3, Transcript length: 828 bps, Translation length: 200 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: F8WCM5

Transcript Support Level (TSL)

TSL:1

Version

ENST00000397270.1

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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