Human (GRCh38.p14)
Description

NCK interacting protein with SH3 domain [Source:HGNC Symbol;Acc:HGNC:15486]

Gene Synonyms

AF3P21, DIP1, ORF1, SPIN90, WASLBP, WISH

Location

Chromosome 3: 48,673,844-48,686,364 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 9 transcripts (splice variants), 199 orthologues and is associated with 36 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000294129.7NCKIPSD-2012977722aaENSP00000294129.2
 
Protein coding
CCDS2776Q9NZQ3-1 NM_016453.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT1TSL:1
ENST00000416649.6NCKIPSD-2042925715aaENSP00000389059.2
 
Protein coding
CCDS46827Q9NZQ3-3 -GENCODE basicAPPRIS P4TSL:1
ENST00000439518.5NCKIPSD-2061214395aaENSP00000409675.1
 
Protein coding
C9JSC3 -TSL:1CDS 3' incomplete
ENST00000426678.1NCKIPSD-205897165aaENSP00000416904.1
 
Protein coding
C9JC20 -TSL:5CDS 3' incomplete
ENST00000453349.5NCKIPSD-207889203aaENSP00000408588.1
 
Protein coding
C9JMQ4 -TSL:3CDS 3' incomplete
ENST00000415281.1NCKIPSD-203803268aaENSP00000406442.1
 
Protein coding
H7C2K2 -TSL:3CDS 5' and 3' incomplete
ENST00000413374.1NCKIPSD-202725151aaENSP00000396683.1
 
Protein coding
H7C0T9 -TSL:3CDS 5' incomplete
ENST00000454134.1NCKIPSD-20899858aaENSP00000416144.1
 
Nonsense mediated decay
F8WCR8 -TSL:3
ENST00000470006.1NCKIPSD-209814No protein-
 
Retained intron
--TSL:2