Human (GRCh38.p14)
Description

nuclear pore complex interacting protein family, member A9 [Source:HGNC Symbol;Acc:HGNC:41984]

Location

Chromosome 16: 18,358,086-18,379,331 reverse strand.

GRCh38:CM000678.2

About this gene

This gene has 9 transcripts (splice variants), 15 orthologues and 19 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000427999.6NPIPA9-2021547369aaENSP00000389275.2
 
Protein coding
CCDS92118A0A0B4J1W7 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000545114.5NPIPA9-2081522232aaENSP00000440825.1
 
Protein coding
--GENCODE basicTSL:1
ENST00000531453.6NPIPA9-205699232aaENSP00000431760.2
 
Protein coding
--GENCODE basicTSL:1
ENST00000528301.1NPIPA9-204671224aaENSP00000437314.1
 
Protein coding
H0YF59 -TSL:2CDS 5' and 3' incomplete
ENST00000327792.6NPIPA9-201462153aaENSP00000331567.5
 
Protein coding
Q9NRE7 -GENCODE basicTSL:NA
ENST00000546267.5NPIPA9-2091495No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000543228.1NPIPA9-207538No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000533010.6NPIPA9-206756No protein-
 
Retained intron
--TSL:3
ENST00000526166.5NPIPA9-203539No protein-
 
Retained intron
--TSL:3