Human (GRCh38.p14)
Description

von Willebrand factor C domain containing 2 [Source:HGNC Symbol;Acc:HGNC:30200]

Gene Synonyms

PSST739, UNQ739

Location
About this transcript

This transcript has 4 exons, is annotated with 23 domains and features, is associated with 62703 variant alleles and maps to 373 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000340652.5VWC2-20111322325aaENSP00000341819.3
 
Protein coding
CCDS5508Q2TAL6 NM_198570.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000855725.1VWC2-2026043325aaENSP00000525784.1
 
Protein coding
CCDS5508--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000855726.1VWC2-2035979325aaENSP00000525785.1
 
Protein coding
CCDS5508--GENCODE BasicAPPRIS P1
ENST00000855727.1VWC2-2044634325aaENSP00000525786.1
 
Protein coding
CCDS5508--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000855728.1VWC2-2052263325aaENSP00000525787.1
 
Protein coding
CCDS5508--GENCODE BasicAPPRIS P1
ENST00000855731.1VWC2-2081948325aaENSP00000525790.1
 
Protein coding
CCDS5508--GENCODE BasicAPPRIS P1
ENST00000855729.1VWC2-2061763325aaENSP00000525788.1
 
Protein coding
CCDS5508--GENCODE BasicAPPRIS P1
ENST00000855730.1VWC2-2071538325aaENSP00000525789.1
 
Protein coding
CCDS5508--GENCODE BasicAPPRIS P1
Statistics

Exons: 4, Coding exons: 3, Transcript length: 11,322 bps, Translation length: 325 residues

MANE

This MANE Select transcript contains ENSP00000341819 and matches to NM_198570.5 and NP_940972.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q2TAL6

CCDS

This transcript is a member of the Human CCDS set: CCDS5508

Transcript Support Level (TSL)

TSL:1

Version

ENST00000340652.5

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.

GENCODE basic gene

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

GENCODE primary gene

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