Canonical Allele Identifier: CA2814904637

Gene: NLRP11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809124_55809125insCACACCCAACAC , CM000681.2:g.55809124_55809125insCACACCCAACAC	GRCh38
NC_000019.9:g.56320490_56320491insCACACCCAACAC , CM000681.1:g.56320490_56320491insCACACCCAACAC	GRCh37
NC_000019.8:g.61012302_61012303insCACACCCAACAC	NCBI36
NG_054722.1:g.32638_32639insGTGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1485_1486insGTGTTGGGTGTG MANE Select	ENSP00000466285.1:p.Ile495_Phe496insValLeuGlyVal
ENST00000589093.5:c.1485_1486insGTGTTGGGTGTG	ENSP00000466285.1:p.Ile495_Phe496insValLeuGlyVal
ENST00000589824.6:c.1485_1486insGTGTTGGGTGTG	ENSP00000468082.1:p.Ile495_Phe496insValLeuGlyVal
ENST00000590409.5:c.1188_1189insGTGTTGGGTGTG	ENSP00000466582.1:p.Ile396_Phe397insValLeuGlyVal
ENST00000592953.5:c.1188_1189insGTGTTGGGTGTG	ENSP00000468196.1:p.Ile396_Phe397insValLeuGlyVal
ENST00000593244.5:c.1485_1486insGTGTTGGGTGTG	ENSP00000467988.1:p.Ile495_Phe496insValLeuGlyVal
NM_001297743.1:c.1188_1189insGTGTTGGGTGTG	NP_001284672.1:p.Ile396_Phe397insValLeuGlyVal
NM_145007.3:c.1485_1486insGTGTTGGGTGTG	NP_659444.2:p.Ile495_Phe496insValLeuGlyVal
NM_001297743.3:c.1188_1189insGTGTTGGGTGTG	NP_001284672.1:p.Ile396_Phe397insValLeuGlyVal
NM_001385451.2:c.1485_1486insGTGTTGGGTGTG	NP_001372380.1:p.Ile495_Phe496insValLeuGlyVal
NM_001385453.2:c.1485_1486insGTGTTGGGTGTG	NP_001372382.1:p.Ile495_Phe496insValLeuGlyVal
NM_145007.5:c.1485_1486insGTGTTGGGTGTG	NP_659444.2:p.Ile495_Phe496insValLeuGlyVal
NR_169620.2:n.1676_1677insGTGTTGGGTGTG
NR_169621.2:n.2009_2010insGTGTTGGGTGTG
NR_169622.2:n.796-7386_796-7385insGTGTTGGGTGTG
NM_001394894.2:c.1485_1486insGTGTTGGGTGTG MANE Select	NP_001381823.1:p.Ile495_Phe496insValLeuGlyVal