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Human (GRCh38.p14)
Description

contactin associated protein 1 [Source:HGNC Symbol;Acc:HGNC:8011]

Gene Synonyms

CASPR, CNTNAP, NRXN4, P190

Location

Chromosome 17: 42,682,531-42,699,993 forward strand.

GRCh38:CM000679.2

About this gene

This gene has 4 transcripts (splice variants), 122 orthologues, 35 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264638.9CNTNAP1-20155371384aaENSP00000264638.3
 
Protein coding
CCDS11436P78357 NM_003632.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000591662.1CNTNAP1-2044499740aaENSP00000466571.1
 
Nonsense mediated decay
K7EMM9 -TSL:1
ENST00000586801.1CNTNAP1-203838No protein-
 
Retained intron
--TSL:3
ENST00000585534.1CNTNAP1-202613No protein-
 
Retained intron
--TSL:3