Human (GRCh38.p14)
Description

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

Gene Synonyms

F8VWF

Location
About this transcript

This transcript has 52 exons, is annotated with 311 domains and features, is associated with 83346 variant alleles and maps to 1755 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: 52, Coding exons: 51, Transcript length: 8,830 bps, Translation length: 2,813 residues

MANE

This MANE Select transcript contains ENSP00000261405 and matches to NM_000552.5 and NP_000543.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: P04275

CCDS

This transcript is a member of the Human CCDS set: CCDS8539

Transcript Support Level (TSL)

TSL:1

Version

ENST00000261405.10

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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