Human (GRCh38.p14)
Description

Wnt family member 2 [Source:HGNC Symbol;Acc:HGNC:12780]

Gene Synonyms

INT1L1, IRP

About this transcript

This transcript has 5 exons, is annotated with 17 domains and features, is associated with 18461 variant alleles and maps to 538 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000265441.8WNT2-2013856360aaENSP00000265441.3
 
Protein coding
CCDS5771A0A384MDX3 P09544 NM_003391.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000491214.1WNT2-204513153aaENSP00000419466.1
 
Protein coding
C9JUI2 -TSL:5CDS 3' incomplete
ENST00000647844.1WNT2-2054205130aaENSP00000497695.1
 
Nonsense mediated decay
A0A3B3ITC9 --
ENST00000449446.5WNT2-2021768110aaENSP00000389643.1
 
Nonsense mediated decay
F8WDR1 -TSL:3
ENST00000461427.1WNT2-203571No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 5, Coding exons: 5, Transcript length: 3,856 bps, Translation length: 360 residues

MANE

This MANE Select transcript contains ENSP00000265441 and matches to NM_003391.3 and NP_003382.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P09544

CCDS

This transcript is a member of the Human CCDS set: CCDS5771

Transcript Support Level (TSL)

TSL:1

Version

ENST00000265441.8

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.