Canonical Allele Identifier: CA509219244
Gene: NLRP11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.56320566C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55809200C>A , CM000681.2:g.55809200C>A GRCh38
NC_000019.9:g.56320566C>A , CM000681.1:g.56320566C>A GRCh37
NC_000019.8:g.61012378C>A NCBI36
NG_054722.1:g.32563G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000589093.6:c.1410G>T MANE Select ENSP00000466285.1:p.Leu470=
ENST00000589093.5:c.1410G>T ENSP00000466285.1:p.Leu470=
ENST00000589824.6:c.1410G>T ENSP00000468082.1:p.Leu470=
ENST00000590409.5:c.1113G>T ENSP00000466582.1:p.Leu371=
ENST00000592953.5:c.1113G>T ENSP00000468196.1:p.Leu371=
ENST00000593244.5:c.1410G>T ENSP00000467988.1:p.Leu470=
NM_001297743.1:c.1113G>T NP_001284672.1:p.Leu371=
NM_145007.3:c.1410G>T NP_659444.2:p.Leu470=
NM_001297743.3:c.1113G>T NP_001284672.1:p.Leu371=
NM_001385451.2:c.1410G>T NP_001372380.1:p.Leu470=
NM_001385453.2:c.1410G>T NP_001372382.1:p.Leu470=
NM_145007.5:c.1410G>T NP_659444.2:p.Leu470=
NR_169620.2:n.1601G>T
NR_169621.2:n.1934G>T
NR_169622.2:n.796-7461G>T
NM_001394894.2:c.1410G>T MANE Select NP_001381823.1:p.Leu470=