Canonical Allele Identifier: CA2343628694

Gene: NLRP11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809048A= , CM000681.2:g.55809048A=	GRCh38
NC_000019.9:g.56320414A= , CM000681.1:g.56320414A=	GRCh37
NC_000019.8:g.61012226A=	NCBI36
NG_054722.1:g.32715T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1562T= MANE Select	ENSP00000466285.1:p.Phe521=
ENST00000589093.5:c.1562T=	ENSP00000466285.1:p.Phe521=
ENST00000589824.6:c.1562T=	ENSP00000468082.1:p.Phe521=
ENST00000590409.5:c.1265T=	ENSP00000466582.1:p.Phe422=
ENST00000592953.5:c.1265T=	ENSP00000468196.1:p.Phe422=
ENST00000593244.5:c.1562T=	ENSP00000467988.1:p.Phe521=
NM_001297743.1:c.1265T=	NP_001284672.1:p.Phe422=
NM_145007.3:c.1562T=	NP_659444.2:p.Phe521=
NM_001297743.3:c.1265T=	NP_001284672.1:p.Phe422=
NM_001385451.2:c.1562T=	NP_001372380.1:p.Phe521=
NM_001385453.2:c.1562T=	NP_001372382.1:p.Phe521=
NM_145007.5:c.1562T=	NP_659444.2:p.Phe521=
NR_169620.2:n.1753T=
NR_169621.2:n.2086T=
NR_169622.2:n.796-7309T=
NM_001394894.2:c.1562T= MANE Select	NP_001381823.1:p.Phe521=