Canonical Allele Identifier: CA2343628684

Gene: NLRP11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809041C= , CM000681.2:g.55809041C=	GRCh38
NC_000019.9:g.56320407C= , CM000681.1:g.56320407C=	GRCh37
NC_000019.8:g.61012219C=	NCBI36
NG_054722.1:g.32722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1569G= MANE Select	ENSP00000466285.1:p.Trp523=
ENST00000589093.5:c.1569G=	ENSP00000466285.1:p.Trp523=
ENST00000589824.6:c.1569G=	ENSP00000468082.1:p.Trp523=
ENST00000590409.5:c.1272G=	ENSP00000466582.1:p.Trp424=
ENST00000592953.5:c.1272G=	ENSP00000468196.1:p.Trp424=
ENST00000593244.5:c.1569G=	ENSP00000467988.1:p.Trp523=
NM_001297743.1:c.1272G=	NP_001284672.1:p.Trp424=
NM_145007.3:c.1569G=	NP_659444.2:p.Trp523=
NM_001297743.3:c.1272G=	NP_001284672.1:p.Trp424=
NM_001385451.2:c.1569G=	NP_001372380.1:p.Trp523=
NM_001385453.2:c.1569G=	NP_001372382.1:p.Trp523=
NM_145007.5:c.1569G=	NP_659444.2:p.Trp523=
NR_169620.2:n.1760G=
NR_169621.2:n.2093G=
NR_169622.2:n.796-7302G=
NM_001394894.2:c.1569G= MANE Select	NP_001381823.1:p.Trp523=