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Human (GRCh38.p14)
Description

NLR family pyrin domain containing 2 [Source:HGNC Symbol;Acc:HGNC:22948]

Gene Synonyms

CLR19.9, FLJ20510, NALP2, NBS1, PAN1, PYPAF2

Location

Scaffold HSCHR19LRC_PGF1_CTG3_1: 869,084-903,922 forward strand.

GRCh38:GL949752.1

View this gene on the primary assembly.

About this gene

This gene has 8 transcripts (splice variants), 1 gene allele and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000620082.2NLRP2-26735731062aaENSP00000484080.1
 
Protein coding
A0A0G2JPQ2 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000618011.3NLRP2-26635071040aaENSP00000478111.1
 
Protein coding
A0A0G2JLX3 -GENCODE BasicTSL:2
ENST00000610346.4NLRP2-26135041039aaENSP00000479218.1
 
Protein coding
A0A0G2JMG8 -GENCODE BasicTSL:2
ENST00000615023.4NLRP2-2632852903aaENSP00000481095.1
 
Protein coding
A0A0G2JNC8 -TSL:5CDS 3' incomplete
ENST00000616079.4NLRP2-2652703879aaENSP00000477745.1
 
Protein coding
A0A0G2JLQ8 -TSL:5CDS 3' incomplete
ENST00000615197.4NLRP2-2642702881aaENSP00000482817.1
 
Protein coding
A0A0G2JP37 -TSL:5CDS 3' incomplete
ENST00000621165.4NLRP2-2683020846aaENSP00000483318.1
 
Nonsense mediated decay
A0A0G2JPB6 -TSL:5
ENST00000611301.1NLRP2-262577No protein-
 
Protein coding CDS not defined
--TSL:4