Human (GRCh37.p13)
Description

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

Gene Synonyms

INSIGF

Location
About this transcript

This transcript has 5 exons, is annotated with 12 domains and features, is associated with 7315 variant alleles and maps to 301 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: 5, Coding exons: 3, Transcript length: 828 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

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000388404 (version 1)
GENCODE basic gene

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