Canonical Allele Identifier: CA2587377239

Gene: NLRP11

Linked Data

• gnomAD v4: 19-55809037-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809038del , CM000681.2:g.55809038del	GRCh38
NC_000019.9:g.56320404del , CM000681.1:g.56320404del	GRCh37
NC_000019.8:g.61012216del	NCBI36
NG_054722.1:g.32725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1572del MANE Select	ENSP00000466285.1:p.Ser525ArgfsTer5
ENST00000589093.5:c.1572del	ENSP00000466285.1:p.Ser525ArgfsTer5
ENST00000589824.6:c.1572del	ENSP00000468082.1:p.Ser525ArgfsTer5
ENST00000590409.5:c.1275del	ENSP00000466582.1:p.Ser426ArgfsTer5
ENST00000592953.5:c.1275del	ENSP00000468196.1:p.Ser426ArgfsTer5
ENST00000593244.5:c.1572del	ENSP00000467988.1:p.Ser525ArgfsTer5
NM_001297743.1:c.1275del	NP_001284672.1:p.Ser426ArgfsTer5
NM_145007.3:c.1572del	NP_659444.2:p.Ser525ArgfsTer5
NM_001297743.3:c.1275del	NP_001284672.1:p.Ser426ArgfsTer5
NM_001385451.2:c.1572del	NP_001372380.1:p.Ser525ArgfsTer5
NM_001385453.2:c.1572del	NP_001372382.1:p.Ser525ArgfsTer5
NM_145007.5:c.1572del	NP_659444.2:p.Ser525ArgfsTer5
NR_169620.2:n.1763del
NR_169621.2:n.2096del
NR_169622.2:n.796-7299del
NM_001394894.2:c.1572del MANE Select	NP_001381823.1:p.Ser525ArgfsTer5