Human (GRCh38.p14)
Description

von Willebrand factor [Source:HGNC Symbol;Acc:HGNC:12726]

Gene Synonyms

F8VWF

Location
About this transcript

This transcript has 3 exons, is associated with 861 variant alleles and maps to 126 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261405.10VWF-20188302813aaENSP00000261405.5
 
Protein coding
CCDS8539P04275-1 NM_000552.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000321023.5VWF-202132660aaENSP00000461331.1
 
Nonsense mediated decay
I3L4K4 -TSL:1
ENST00000538563.1VWF-20370960aaENSP00000459134.1
 
Nonsense mediated decay
I3L4K4 -TSL:3
ENST00000545906.1VWF-207745No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000539641.1VWF-205688No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000540192.1VWF-206579No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000538635.5VWF-204475No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000621700.1VWF-209556No protein-
 
Retained intron
--TSL:3
ENST00000612016.1VWF-208535No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 3, Coding exons: 0, Transcript length: 579 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000540192.1

Type

Protein coding CDS not defined

Annotation Method

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

Annotation Attributes

dotter confirmed [Definitions]