Canonical Allele Identifier: CA2587377246
Gene: NLRP11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55809137_55809138insTCTG , CM000681.2:g.55809137_55809138insTCTG GRCh38
NC_000019.9:g.56320503_56320504insTCTG , CM000681.1:g.56320503_56320504insTCTG GRCh37
NC_000019.8:g.61012315_61012316insTCTG NCBI36
NG_054722.1:g.32625_32626insCAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000589093.6:c.1472_1473insCAGA MANE Select ENSP00000466285.1:p.Phe492ArgfsTer18
ENST00000589093.5:c.1472_1473insCAGA ENSP00000466285.1:p.Phe492ArgfsTer18
ENST00000589824.6:c.1472_1473insCAGA ENSP00000468082.1:p.Phe492ArgfsTer18
ENST00000590409.5:c.1175_1176insCAGA ENSP00000466582.1:p.Phe393ArgfsTer18
ENST00000592953.5:c.1175_1176insCAGA ENSP00000468196.1:p.Phe393ArgfsTer18
ENST00000593244.5:c.1472_1473insCAGA ENSP00000467988.1:p.Phe492ArgfsTer18
NM_001297743.1:c.1175_1176insCAGA NP_001284672.1:p.Phe393ArgfsTer18
NM_145007.3:c.1472_1473insCAGA NP_659444.2:p.Phe492ArgfsTer18
NM_001297743.3:c.1175_1176insCAGA NP_001284672.1:p.Phe393ArgfsTer18
NM_001385451.2:c.1472_1473insCAGA NP_001372380.1:p.Phe492ArgfsTer18
NM_001385453.2:c.1472_1473insCAGA NP_001372382.1:p.Phe492ArgfsTer18
NM_145007.5:c.1472_1473insCAGA NP_659444.2:p.Phe492ArgfsTer18
NR_169620.2:n.1663_1664insCAGA
NR_169621.2:n.1996_1997insCAGA
NR_169622.2:n.796-7399_796-7398insCAGA
NM_001394894.2:c.1472_1473insCAGA MANE Select NP_001381823.1:p.Phe492ArgfsTer18