Human (GRCh38.p14)
Description

WD repeat domain 17 [Source:HGNC Symbol;Acc:HGNC:16661]

About this transcript

This transcript has 4 exons, is associated with 2072 variant alleles and maps to 99 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000508596.6WDR17-20573331283aaENSP00000422763.1
 
Protein coding
CCDS43284Q8IZU2-2 NM_181265.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000443118.3WDR17-2024911557aaENSP00000426985.1
 
Protein coding
H0YAG1 -TSL:1CDS 5' incomplete
ENST00000280190.8WDR17-20147051322aaENSP00000280190.4
 
Protein coding
CCDS3825Q8IZU2-1 -GENCODE basicTSL:1
ENST00000507824.6WDR17-20441191297aaENSP00000422200.2
 
Protein coding
E7ESC9 -GENCODE basicTSL:5
ENST00000505894.2WDR17-203677226aaENSP00000426847.2
 
Protein coding
H0YAE4 -TSL:5CDS 5' and 3' incomplete
ENST00000513261.1WDR17-208466101aaENSP00000427502.1
 
Nonsense mediated decay
E9PFA2 -TSL:3
ENST00000509792.1WDR17-207456No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000508773.1WDR17-206485No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 4, Coding exons: 0, Transcript length: 485 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000508773.1

Type

Retained intron

Annotation Method

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