Human (GRCh38.p14)
Description

insulin induced gene 2 [Source:HGNC Symbol;Acc:HGNC:20452]

About this transcript

This transcript has 6 exons, is annotated with 12 domains and features, is associated with 9588 variant alleles and maps to 385 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000245787.9INSIG2-2013562225aaENSP00000245787.4
 
Protein coding
CCDS2122A0A024RAI2 Q9Y5U4 NM_016133.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000411929.5INSIG2-20257439aaENSP00000400126.1
 
Nonsense mediated decay
F8WCG8 -TSL:2
ENST00000485520.5INSIG2-2063185No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000471186.5INSIG2-2042100No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000467223.5INSIG2-203627No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000479999.1INSIG2-205532No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000488995.1INSIG2-207518No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 6, Coding exons: 5, Transcript length: 3,562 bps, Translation length: 225 residues

MANE

This MANE Select transcript contains ENSP00000245787 and matches to NM_016133.4 and NP_057217.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y5U4

CCDS

This transcript is a member of the Human CCDS set: CCDS2122

Transcript Support Level (TSL)

TSL:1

Version

ENST00000245787.9

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.