Human (GRCh37.p13)
Description

contactin 5 [Source:HGNC Symbol;Acc:2175]

Gene Synonyms

HNB-2s, NB-2, hNB-2

About this transcript

This transcript has 23 exons, is annotated with 61 domains and features, is associated with 408223 variant alleles and maps to 636 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000524871.1CNTN5-00162581100aaENSP00000435637.1
 
Protein coding
CCDS53696B4DGP0 O94779 NM_014361.3GENCODE basic
ENST00000527185.1CNTN5-0034303911aaENSP00000433575.1
 
Protein coding
CCDS58168O94779 NM_001243271.1GENCODE basic
ENST00000528682.1CNTN5-00638001100aaENSP00000436185.1
 
Protein coding
CCDS53696B4DGP0 O94779 NM_001243270.1GENCODE basic
ENST00000418526.2CNTN5-00436791026aaENSP00000393229.2
 
Protein coding
CCDS53697B4DGP0 O94779 NM_175566.2GENCODE basic
ENST00000279463.3CNTN5-20133031100aaENSP00000279463.3
 
Protein coding
CCDS53696B4DGP0 O94779 -GENCODE basic
ENST00000530458.1CNTN5-00824659aaENSP00000433558.1
 
Protein coding
E9PKF9 -CDS 3' incomplete
ENST00000524560.1CNTN5-0051620No protein-
 
Processed transcript
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ENST00000525047.1CNTN5-007572No protein-
 
Processed transcript
---
ENST00000525236.1CNTN5-009474No protein-
 
Processed transcript
---
ENST00000528727.1CNTN5-0023144No protein-
 
Retained intron
---
ENST00000527682.1CNTN5-010553No protein-
 
Retained intron
---
Statistics

Exons: 23, Coding exons: 23, Transcript length: 3,303 bps, Translation length: 1,100 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: O94779

CCDS

This transcript is a member of the Human CCDS set: CCDS53696

Version

ENST00000279463.3

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

Stop codons

This transcript has a variant, rs12292659, that causes a stop codon to be gained in at least 10% of HapMap or 1000 Genome population(s) CSHL-HAPMAP:HapMap-CEU, ESP6500:African_American, CSHL-HAPMAP:HapMap-YRI, ESP6500:European_American, CSHL-HAPMAP:HapMap-HCB.

GENCODE basic gene

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