Human (GRCh38.p14)
Description

nuclear pore complex interacting protein family member A2 [Source:HGNC Symbol;Acc:HGNC:41979]

Location
About this transcript

This transcript has 10 exons, is annotated with 8 domains and features, is associated with 2058 variant alleles and maps to 2753 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000529166.6NPIPA2-2011509369aaENSP00000432029.1
 
Protein coding
CCDS92115E9PIF3 NM_001395485.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000553201.1NPIPA2-2031053350aaENSP00000446882.1
 
Protein coding
CCDS59263A0A0B4J2F6 -GENCODE BasicTSL:1
ENST00000530328.5NPIPA2-202954317aaENSP00000432767.1
 
Protein coding
E9PNS9 -GENCODE PrimaryGENCODE BasicTSL:5
Statistics

Exons: 10, Coding exons: 8, Transcript length: 1,509 bps, Translation length: 369 residues

MANE

This MANE Select transcript contains ENSP00000432029 and matches to NM_001395485.2 and NP_001382414.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: E9PIF3

CCDS

This transcript is a member of the Human CCDS set: CCDS92115

Transcript Support Level (TSL)

TSL:5

Version

ENST00000529166.6

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Annotation Attributes

RNA-Seq supported partial [Definitions]

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.