Human (GRCh38.p14)
Description

villin like [Source:HGNC Symbol;Acc:HGNC:30906]

Location
About this transcript

This transcript has 20 exons, is annotated with 49 domains and features, is associated with 9046 variant alleles and maps to 622 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000383759.7VILL-2022831856aaENSP00000373266.2
 
Protein coding
CCDS2670O15195-1 NM_015873.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000283713.10VILL-2012970856aaENSP00000283713.6
 
Protein coding
CCDS2670O15195-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000465644.5VILL-2061857574aaENSP00000422096.1
 
Protein coding
D6R9H2 -GENCODE basicTSL:5
ENST00000492491.6VILL-210686187aaENSP00000427355.1
 
Protein coding
E9PFV5 -TSL:5CDS 3' incomplete
ENST00000412008.5VILL-203813101aaENSP00000387659.1
 
Nonsense mediated decay
H7BZ43 -TSL:3CDS 5' incomplete
ENST00000486616.5VILL-2084439No protein-
 
Retained intron
--TSL:2
ENST00000484717.5VILL-2072072No protein-
 
Retained intron
--TSL:1
ENST00000463080.2VILL-205831No protein-
 
Retained intron
--TSL:5
ENST00000488209.1VILL-209543No protein-
 
Retained intron
--TSL:2
ENST00000460040.1VILL-204448No protein-
 
Retained intron
--TSL:3

Protein domains for ENSP00000283713.6