Canonical Allele Identifier: CA407586461
Gene: NLRP11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55809128G>T , CM000681.2:g.55809128G>T GRCh38
NC_000019.9:g.56320494G>T , CM000681.1:g.56320494G>T GRCh37
NC_000019.8:g.61012306G>T NCBI36
NG_054722.1:g.32635C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000589093.6:c.1482C>A MANE Select ENSP00000466285.1:p.Phe494Leu
ENST00000589093.5:c.1482C>A ENSP00000466285.1:p.Phe494Leu
ENST00000589824.6:c.1482C>A ENSP00000468082.1:p.Phe494Leu
ENST00000590409.5:c.1185C>A ENSP00000466582.1:p.Phe395Leu
ENST00000592953.5:c.1185C>A ENSP00000468196.1:p.Phe395Leu
ENST00000593244.5:c.1482C>A ENSP00000467988.1:p.Phe494Leu
NM_001297743.1:c.1185C>A NP_001284672.1:p.Phe395Leu
NM_145007.3:c.1482C>A NP_659444.2:p.Phe494Leu
NM_001297743.3:c.1185C>A NP_001284672.1:p.Phe395Leu
NM_001385451.2:c.1482C>A NP_001372380.1:p.Phe494Leu
NM_001385453.2:c.1482C>A NP_001372382.1:p.Phe494Leu
NM_145007.5:c.1482C>A NP_659444.2:p.Phe494Leu
NR_169620.2:n.1673C>A
NR_169621.2:n.2006C>A
NR_169622.2:n.796-7389C>A
NM_001394894.2:c.1482C>A MANE Select NP_001381823.1:p.Phe494Leu