Human (GRCh38.p14)
Description

WD repeat domain 13 [Source:HGNC Symbol;Acc:HGNC:14352]

Location
About this transcript

This transcript has 10 exons, is annotated with 18 domains and features, is associated with 4369 variant alleles and maps to 578 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000376729.10WDR13-2025457485aaENSP00000365919.5
 
Protein coding
CCDS14302Q9H1Z4 NM_001347217.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000218056.9WDR13-2012124485aaENSP00000218056.5
 
Protein coding
CCDS14302Q9H1Z4 -GENCODE basicAPPRIS P1TSL:1
ENST00000482760.3WDR13-207562187aaENSP00000483191.1
 
Protein coding
A0A087X091 -TSL:3CDS 5' and 3' incomplete
ENST00000470124.1WDR13-204437107aaENSP00000480532.1
 
Protein coding
A0A087WWV5 -TSL:3CDS 3' incomplete
ENST00000486125.5WDR13-20893643aaENSP00000482667.1
 
Nonsense mediated decay
A0A087X2H9 -TSL:2
ENST00000498631.5WDR13-21285943aaENSP00000484996.1
 
Nonsense mediated decay
A0A087X2H9 -TSL:2
ENST00000492715.1WDR13-2092612No protein-
 
Retained intron
--TSL:5
ENST00000479279.5WDR13-2062486No protein-
 
Retained intron
--TSL:1
ENST00000466962.1WDR13-203684No protein-
 
Retained intron
--TSL:3
ENST00000495575.1WDR13-211547No protein-
 
Retained intron
--TSL:2
ENST00000492873.1WDR13-210470No protein-
 
Retained intron
--TSL:2
ENST00000472440.1WDR13-205430No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 10, Coding exons: 9, Transcript length: 5,457 bps, Translation length: 485 residues

MANE

This MANE Select transcript contains ENSP00000365919 and matches to NM_001347217.2 and NP_001334146.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9H1Z4

CCDS

This transcript is a member of the Human CCDS set: CCDS14302

Transcript Support Level (TSL)

TSL:5

Version

ENST00000376729.10

Type

Protein coding

Annotation Method

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

GENCODE basic gene

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