Human (GRCh37.p13)
Description

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

Gene Synonyms

FLJ32009, URG11, VWC1

Location
About this transcript

This transcript has 20 exons, is annotated with 70 domains and features, is associated with 16533 variant alleles and maps to 569 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000335613.5VWCE-0013640955aaENSP00000334186.5
 
Protein coding
CCDS8002B4DY31 Q96DN2 NM_152718.2GENCODE basic
ENST00000535710.1VWCE-0041437420aaENSP00000442570.1
 
Protein coding
B4DY31 -GENCODE basic
ENST00000301770.6VWCE-0023364219aaENSP00000301770.6
 
Nonsense mediated decay
Q96DN2 --
ENST00000535599.1VWCE-003883173aaENSP00000441565.1
 
Nonsense mediated decay
B4DS56 --
ENST00000538438.1VWCE-0061076No protein-
 
Retained intron
---
ENST00000398808.3VWCE-005717No protein-
 
Retained intron
---
ENST00000538579.1VWCE-007581No protein-
 
Retained intron
---
Statistics

Exons: 20, Coding exons: 20, Transcript length: 3,640 bps, Translation length: 955 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96DN2

CCDS

This transcript is a member of the Human CCDS set: CCDS8002

Version

ENST00000335613.5

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000398811 (version 1)
GENCODE basic gene

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