Human (GRCh38.p14)
Description

von Willebrand factor C and EGF domains [Source:HGNC Symbol;Acc:HGNC:26487]

Gene Synonyms

FLJ32009, URG11, VWC1

Location
About this transcript

This transcript has 2 exons, is associated with 1109 variant alleles and maps to 66 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000335613.10VWCE-2023536955aaENSP00000334186.5
 
Protein coding
CCDS8002Q96DN2-1 NM_152718.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000535710.1VWCE-2051437420aaENSP00000442570.1
 
Protein coding
B4DY31 -GENCODE basicTSL:2
ENST00000301770.10VWCE-2013368219aaENSP00000301770.6
 
Nonsense mediated decay
Q96DN2-2 -TSL:1
ENST00000535599.1VWCE-204883173aaENSP00000441565.1
 
Nonsense mediated decay
B4DS56 -TSL:2
ENST00000538438.1VWCE-2061076No protein-
 
Retained intron
--TSL:3
ENST00000398808.3VWCE-203717No protein-
 
Retained intron
--TSL:3
ENST00000538579.1VWCE-207581No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 2, Coding exons: 0, Transcript length: 717 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000398808.3

Type

Retained intron

Annotation Method

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