Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 5 exons, is associated with 1921 variant alleles and maps to 194 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
Statistics

Exons: 5, Coding exons: 0, Transcript length: 831 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000463080.2

Type

Retained intron

Annotation Method

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