Human (GRCh37.p13)
Description

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

Gene Synonyms

INSIGF

Location
About this transcript

This transcript has 7 exons, is annotated with 12 domains and features, is associated with 15327 variant alleles and maps to 689 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000397270.1INS-IGF2-001828200aaENSP00000380440.1
 
Protein coding
CCDS41598F8WCM5 NM_001042376.2Ensembl CanonicalGENCODE basic
ENST00000356578.4INS-IGF2-0021706200aaENSP00000348986.4
 
Nonsense mediated decay
CCDS41598F8WCM5 --
ENST00000481781.1INS-IGF2-003977No protein-
 
Processed transcript
---
ENST00000476874.1INS-IGF2-005482No protein-
 
Retained intron
---
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

CCDS

This transcript is a member of the Human CCDS set: CCDS41598

Version

ENST00000356578.4

Type

Nonsense mediated decay

Annotation Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000026061 (version 1)