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Human (GRCh38.p14)
Description

nuclear pore complex interacting protein family member B12 [Source:HGNC Symbol;Acc:HGNC:37491]

Location

Chromosome 16: 29,483,534-29,506,408 reverse strand.

GRCh38:CM000678.2

About this gene

This gene has 7 transcripts (splice variants), 28 orthologues and 19 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000550665.6NPIPB12-2043605928aaENSP00000447597.2
 
Protein coding
F8W0I5 NM_001395931.1MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000551448.5NPIPB12-20691040aaENSP00000449771.1
 
Nonsense mediated decay
F5GWQ4 -TSL:3
ENST00000549733.5NPIPB12-20379768aaENSP00000449873.1
 
Nonsense mediated decay
H0YIQ5 -TSL:4CDS 5' incomplete
ENST00000547235.5NPIPB12-20171024aaENSP00000449585.1
 
Nonsense mediated decay
H0YIK9 -TSL:3CDS 5' incomplete
ENST00000550690.1NPIPB12-20567549aaENSP00000449726.1
 
Nonsense mediated decay
E5RHP9 -TSL:5
ENST00000552123.1NPIPB12-20746478aaENSP00000449864.1
 
Nonsense mediated decay
H0YIQ3 -TSL:4CDS 5' incomplete
ENST00000548346.1NPIPB12-202611No protein-
 
Retained intron
--TSL:2