Human (GRCh38.p14)
Description

NBPF member 26 [Source:HGNC Symbol;Acc:HGNC:49571]

Location

Chromosome 1: 120,723,945-120,842,229 forward strand.

GRCh38:CM000663.2

View alleles of this gene on alternative sequences

About this gene

This gene has 8 transcripts (splice variants), 1 gene allele, 68 orthologues and 14 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000620612.6NBPF26-20468911673aaENSP00000481542.4
 
Protein coding
A0A087WY62 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000711669.1NBPF26-2083059913aaENSP00000518829.1
 
Protein coding
--CDS 5' incomplete
ENST00000611287.5NBPF26-2012969942aaENSP00000482859.2
 
Protein coding
A0A087WZS8 -GENCODE basicTSL:5
ENST00000611702.5NBPF26-2022931942aaENSP00000478334.2
 
Protein coding
A0A087WU30 -GENCODE basicTSL:5
ENST00000617913.5NBPF26-2032701867aaENSP00000480416.2
 
Protein coding
A0A087WWQ1 -GENCODE basicTSL:5
ENST00000651062.1NBPF26-2052182727aaENSP00000498447.1
 
Protein coding
A0A494C0A2 -CDS 5' and 3' incomplete
ENST00000652763.1NBPF26-207139177aaENSP00000498974.1
 
Protein coding
A0A494C1A6 -CDS 3' incomplete
ENST00000652444.2NBPF26-2064458598aaENSP00000498391.2
 
Nonsense mediated decay
A0A494C053 --