Canonical Allele Identifier: CA2343628699

Gene: NLRP11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809054T= , CM000681.2:g.55809054T=	GRCh38
NC_000019.9:g.56320420T= , CM000681.1:g.56320420T=	GRCh37
NC_000019.8:g.61012232T=	NCBI36
NG_054722.1:g.32709A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1556A= MANE Select	ENSP00000466285.1:p.Asp519=
ENST00000589093.5:c.1556A=	ENSP00000466285.1:p.Asp519=
ENST00000589824.6:c.1556A=	ENSP00000468082.1:p.Asp519=
ENST00000590409.5:c.1259A=	ENSP00000466582.1:p.Asp420=
ENST00000592953.5:c.1259A=	ENSP00000468196.1:p.Asp420=
ENST00000593244.5:c.1556A=	ENSP00000467988.1:p.Asp519=
NM_001297743.1:c.1259A=	NP_001284672.1:p.Asp420=
NM_145007.3:c.1556A=	NP_659444.2:p.Asp519=
NM_001297743.3:c.1259A=	NP_001284672.1:p.Asp420=
NM_001385451.2:c.1556A=	NP_001372380.1:p.Asp519=
NM_001385453.2:c.1556A=	NP_001372382.1:p.Asp519=
NM_145007.5:c.1556A=	NP_659444.2:p.Asp519=
NR_169620.2:n.1747A=
NR_169621.2:n.2080A=
NR_169622.2:n.796-7315A=
NM_001394894.2:c.1556A= MANE Select	NP_001381823.1:p.Asp519=