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Human (GRCh38.p14)
Description

Wnt family member 7B [Source:HGNC Symbol;Acc:HGNC:12787]

Location
About this transcript

This transcript has 4 exons, is annotated with 24 domains and features, is associated with 32507 variant alleles and maps to 408 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000339464.9WNT7B-2013948349aaENSP00000341032.4
 
Protein coding
CCDS33667P56706 NM_058238.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P4TSL:1
ENST00000409496.7WNT7B-2022285353aaENSP00000386546.3
 
Protein coding
CCDS93177A8K0G1 -GENCODE BasicAPPRIS ALT1TSL:2
ENST00000410089.5WNT7B-2042202333aaENSP00000386781.1
 
Protein coding
B8A595 -GENCODE PrimaryGENCODE BasicTSL:5
ENST00000410058.1WNT7B-203714205aaENSP00000387217.1
 
Protein coding
B8A597 -GENCODE BasicTSL:3
ENST00000428540.1WNT7B-20552157aaENSP00000392750.1
 
Protein coding
B8A598 -TSL:3CDS 3' incomplete
Statistics

Exons: 4, Coding exons: 4, Transcript length: 3,948 bps, Translation length: 349 residues

MANE

This MANE Select transcript contains ENSP00000341032 and matches to NM_058238.3 and NP_478679.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P56706

CCDS

This transcript is a member of the Human CCDS set: CCDS33667

Transcript Support Level (TSL)

TSL:1

Version

ENST00000339464.9

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.

GENCODE primary gene

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