Canonical Allele Identifier: CA509219234

Gene: NLRP11

Linked Data

• MyVariant Identifiers: chr19:g.56320560G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809194G>T , CM000681.2:g.55809194G>T	GRCh38
NC_000019.9:g.56320560G>T , CM000681.1:g.56320560G>T	GRCh37
NC_000019.8:g.61012372G>T	NCBI36
NG_054722.1:g.32569C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1416C>A MANE Select	ENSP00000466285.1:p.Pro472=
ENST00000589093.5:c.1416C>A	ENSP00000466285.1:p.Pro472=
ENST00000589824.6:c.1416C>A	ENSP00000468082.1:p.Pro472=
ENST00000590409.5:c.1119C>A	ENSP00000466582.1:p.Pro373=
ENST00000592953.5:c.1119C>A	ENSP00000468196.1:p.Pro373=
ENST00000593244.5:c.1416C>A	ENSP00000467988.1:p.Pro472=
NM_001297743.1:c.1119C>A	NP_001284672.1:p.Pro373=
NM_145007.3:c.1416C>A	NP_659444.2:p.Pro472=
NM_001297743.3:c.1119C>A	NP_001284672.1:p.Pro373=
NM_001385451.2:c.1416C>A	NP_001372380.1:p.Pro472=
NM_001385453.2:c.1416C>A	NP_001372382.1:p.Pro472=
NM_145007.5:c.1416C>A	NP_659444.2:p.Pro472=
NR_169620.2:n.1607C>A
NR_169621.2:n.1940C>A
NR_169622.2:n.796-7455C>A
NM_001394894.2:c.1416C>A MANE Select	NP_001381823.1:p.Pro472=