Canonical Allele Identifier: CA2587377244

Gene: NLRP11

Linked Data

• gnomAD v4: 19-55809098-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809101_55809103del , CM000681.2:g.55809101_55809103del	GRCh38
NC_000019.9:g.56320467_56320469del , CM000681.1:g.56320467_56320469del	GRCh37
NC_000019.8:g.61012279_61012281del	NCBI36
NG_054722.1:g.32662_32664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1509_1511del MANE Select	ENSP00000466285.1:p.Arg504del
ENST00000589093.5:c.1509_1511del	ENSP00000466285.1:p.Arg504del
ENST00000589824.6:c.1509_1511del	ENSP00000468082.1:p.Arg504del
ENST00000590409.5:c.1212_1214del	ENSP00000466582.1:p.Arg405del
ENST00000592953.5:c.1212_1214del	ENSP00000468196.1:p.Arg405del
ENST00000593244.5:c.1509_1511del	ENSP00000467988.1:p.Arg504del
NM_001297743.1:c.1212_1214del	NP_001284672.1:p.Arg405del
NM_145007.3:c.1509_1511del	NP_659444.2:p.Arg504del
NM_001297743.3:c.1212_1214del	NP_001284672.1:p.Arg405del
NM_001385451.2:c.1509_1511del	NP_001372380.1:p.Arg504del
NM_001385453.2:c.1509_1511del	NP_001372382.1:p.Arg504del
NM_145007.5:c.1509_1511del	NP_659444.2:p.Arg504del
NR_169620.2:n.1700_1702del
NR_169621.2:n.2033_2035del
NR_169622.2:n.796-7362_796-7360del
NM_001394894.2:c.1509_1511del MANE Select	NP_001381823.1:p.Arg504del