Canonical Allele Identifier: CA509219236

Gene: NLRP11

Linked Data

• MyVariant Identifiers: chr19:g.56320563G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55809197G>A , CM000681.2:g.55809197G>A	GRCh38
NC_000019.9:g.56320563G>A , CM000681.1:g.56320563G>A	GRCh37
NC_000019.8:g.61012375G>A	NCBI36
NG_054722.1:g.32566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589093.6:c.1413C>T MANE Select	ENSP00000466285.1:p.Ile471=
ENST00000589093.5:c.1413C>T	ENSP00000466285.1:p.Ile471=
ENST00000589824.6:c.1413C>T	ENSP00000468082.1:p.Ile471=
ENST00000590409.5:c.1116C>T	ENSP00000466582.1:p.Ile372=
ENST00000592953.5:c.1116C>T	ENSP00000468196.1:p.Ile372=
ENST00000593244.5:c.1413C>T	ENSP00000467988.1:p.Ile471=
NM_001297743.1:c.1116C>T	NP_001284672.1:p.Ile372=
NM_145007.3:c.1413C>T	NP_659444.2:p.Ile471=
NM_001297743.3:c.1116C>T	NP_001284672.1:p.Ile372=
NM_001385451.2:c.1413C>T	NP_001372380.1:p.Ile471=
NM_001385453.2:c.1413C>T	NP_001372382.1:p.Ile471=
NM_145007.5:c.1413C>T	NP_659444.2:p.Ile471=
NR_169620.2:n.1604C>T
NR_169621.2:n.1937C>T
NR_169622.2:n.796-7458C>T
NM_001394894.2:c.1413C>T MANE Select	NP_001381823.1:p.Ile471=