Human (GRCh37.p13) ▼
Description

NLR family, pyrin domain containing 1 [Source:HGNC Symbol;Acc:14374]

Gene Synonyms

CARD7, CIDED, CLR17.1, DEFCAP, DEFCAP-L/S, DKFZp586O1822, KIAA0926, NAC, NALP1, PP1044, SLEV1, VAMAS1

Location

Chromosome 17: 5,402,747-5,522,744 reverse strand.

GRCh37:CM000679.1

About this gene

This gene has 14 transcripts (splice variants), 96 orthologues, 20 paralogues and is associated with 7 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000572272.1NLRP1-01144221473aaENSP00000460475.1
 
Protein coding
CCDS42246I3L0S2 I3L2G5 Q9C000
-Ensembl CanonicalGENCODE Basic
ENST00000345221.3NLRP1-20154801429aaENSP00000324366.3
 
Protein coding
CCDS42245I3L0S2 I3L2G5 Q9C000
NM_033007.3GENCODE Basic
ENST00000262467.5NLRP1-00151311375aaENSP00000262467.5
 
Protein coding
CCDS32537E9PE50 I3L0S2 Q9H5Z7
NM_001033053.2GENCODE Basic
ENST00000269280.4NLRP1-01050751429aaENSP00000269280.4
 
Protein coding
CCDS42245I3L0S2 I3L2G5 Q9C000
-GENCODE Basic
ENST00000354411.3NLRP1-01243321443aaENSP00000346390.3
 
Protein coding
CCDS42244I3L0S2 Q9C000 NM_033006.3GENCODE Basic
ENST00000577119.1NLRP1-00942001399aaENSP00000460216.1
 
Protein coding
CCDS58508I3L0S2 Q9C000 -GENCODE Basic
ENST00000576905.1NLRP1-01455535aaENSP00000458303.1
 
Protein coding
I3L0S2 -CDS 3' incomplete
ENST00000571451.2NLRP1-00854441051aaENSP00000459661.2
 
Nonsense mediated decay
I3L0S2 I3L2G5 --
ENST00000544378.2NLRP1-00252811375aaENSP00000442029.2
 
Nonsense mediated decay
CCDS32537E9PE50 I3L0S2 Q9H5Z7
--
ENST00000571307.1NLRP1-0074050No protein-
 
Processed transcript
---
ENST00000574406.1NLRP1-0031750No protein-
 
Processed transcript
---
ENST00000568641.1NLRP1-0041627No protein-
 
Processed transcript
---
ENST00000572143.1NLRP1-013578No protein-
 
Processed transcript
---
ENST00000574512.1NLRP1-0054506No protein-
 
Retained intron
---

Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.