Canonical Allele Identifier: CA2587377249
Gene: NLRP11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55809284_55809285del , CM000681.2:g.55809284_55809285del GRCh38
NC_000019.9:g.56320650_56320651del , CM000681.1:g.56320650_56320651del GRCh37
NC_000019.8:g.61012462_61012463del NCBI36
NG_054722.1:g.32479_32480del

Transcript Alleles

HGVS Amino-acid Change
ENST00000589093.6:c.1326_1327del MANE Select ENSP00000466285.1:p.His442GlnfsTer?
ENST00000589093.5:c.1326_1327del ENSP00000466285.1:p.His442GlnfsTer?
ENST00000589824.6:c.1326_1327del ENSP00000468082.1:p.His442GlnfsTer?
ENST00000590409.5:c.1029_1030del ENSP00000466582.1:p.His343GlnfsTer?
ENST00000592953.5:c.1029_1030del ENSP00000468196.1:p.His343GlnfsTer?
ENST00000593244.5:c.1326_1327del ENSP00000467988.1:p.His442GlnfsTer?
NM_001297743.1:c.1029_1030del NP_001284672.1:p.His343GlnfsTer?
NM_145007.3:c.1326_1327del NP_659444.2:p.His442GlnfsTer?
NM_001297743.3:c.1029_1030del NP_001284672.1:p.His343GlnfsTer?
NM_001385451.2:c.1326_1327del NP_001372380.1:p.His442GlnfsTer?
NM_001385453.2:c.1326_1327del NP_001372382.1:p.His442GlnfsTer?
NM_145007.5:c.1326_1327del NP_659444.2:p.His442GlnfsTer?
NR_169620.2:n.1517_1518del
NR_169621.2:n.1850_1851del
NR_169622.2:n.796-7545_796-7544del
NM_001394894.2:c.1326_1327del MANE Select NP_001381823.1:p.His442GlnfsTer?