Canonical Allele Identifier: CA16044250
Gene: NLRP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375414
dbSNP Id: rs1057519493

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5583761G>A , CM000679.2:g.5583761G>A GRCh38
NC_000017.10:g.5487081G>A , CM000679.1:g.5487081G>A GRCh37
NC_000017.9:g.5427805G>A NCBI36
NG_011651.1:g.5752C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262467.11:c.197C>T ENSP00000262467.5:p.Ala66Val
ENST00000269280.9:c.197C>T ENSP00000269280.4:p.Ala66Val
ENST00000354411.8:c.197C>T ENSP00000346390.3:p.Ala66Val
ENST00000544378.7:c.197C>T ENSP00000442029.2:p.Ala66Val
ENST00000571307.2:c.197C>T ENSP00000514459.1:p.Ala66Val
ENST00000571451.7:c.197C>T ENSP00000459661.3:p.Ala66Val
ENST00000572143.2:c.197C>T ENSP00000514476.1:p.Ala66Val
ENST00000576905.6:c.197C>T ENSP00000458303.2:p.Ala66Val
ENST00000617618.5:c.197C>T ENSP00000478516.1:p.Ala66Val
ENST00000699586.1:c.197C>T ENSP00000514458.1:p.Ala66Val
ENST00000699613.1:c.197C>T ENSP00000514477.1:p.Ala66Val
ENST00000699614.1:c.197C>T ENSP00000514478.1:p.Ala66Val
ENST00000699615.1:c.197C>T ENSP00000514479.1:p.Ala66Val
ENST00000699623.1:c.197C>T ENSP00000514483.1:p.Ala66Val
ENST00000699625.1:c.197C>T ENSP00000514484.1:p.Ala66Val
ENST00000699626.1:c.197C>T ENSP00000514485.1:p.Ala66Val
ENST00000699629.1:c.197C>T ENSP00000514488.1:p.Ala66Val
ENST00000699630.1:c.197C>T ENSP00000514489.1:p.Ala66Val
ENST00000699632.1:c.197C>T ENSP00000514490.1:p.Ala66Val
ENST00000699633.1:c.197C>T ENSP00000514491.1:p.Ala66Val
ENST00000699634.1:c.197C>T ENSP00000514492.1:p.Ala66Val
ENST00000699636.1:n.731C>T
ENST00000699638.1:n.453C>T
ENST00000699642.1:c.197C>T ENSP00000514495.1:p.Ala66Val
ENST00000699643.1:c.115+82C>T ENSP00000514496.1:n.115+82C>T
ENST00000699644.1:c.197C>T ENSP00000514497.1:p.Ala66Val
ENST00000699645.1:c.197C>T ENSP00000514498.1:p.Ala66Val
ENST00000699665.1:c.197C>T ENSP00000514508.1:p.Ala66Val
ENST00000699705.1:c.197C>T ENSP00000514530.1:p.Ala66Val
ENST00000699707.1:c.197C>T ENSP00000514532.1:p.Ala66Val
ENST00000699708.1:c.197C>T ENSP00000514533.1:p.Ala66Val
ENST00000699709.1:c.197C>T ENSP00000514534.1:p.Ala66Val
ENST00000699710.1:c.197C>T ENSP00000514535.1:p.Ala66Val
ENST00000699711.1:c.197C>T ENSP00000514536.1:p.Ala66Val
ENST00000699712.1:c.197C>T ENSP00000514537.1:p.Ala66Val
ENST00000699713.1:c.197C>T ENSP00000514538.1:p.Ala66Val
ENST00000699775.1:c.197C>T ENSP00000514581.1:p.Ala66Val
ENST00000699776.1:c.197C>T ENSP00000514582.1:p.Ala66Val
ENST00000699777.1:c.197C>T ENSP00000514583.1:p.Ala66Val
ENST00000699809.1:c.197C>T ENSP00000514612.1:p.Ala66Val
ENST00000699810.1:c.197C>T ENSP00000514613.1:p.Ala66Val
ENST00000262467.10:c.197C>T ENSP00000262467.5:p.Ala66Val
ENST00000572272.6:c.197C>T MANE Select ENSP00000460475.1:p.Ala66Val
ENST00000262467.9:c.197C>T ENSP00000262467.5:p.Ala66Val
ENST00000269280.8:c.197C>T ENSP00000269280.4:p.Ala66Val
ENST00000345221.7:c.197C>T ENSP00000324366.3:p.Ala66Val
ENST00000354411.7:c.197C>T ENSP00000346390.3:p.Ala66Val
ENST00000544378.6:c.197C>T ENSP00000442029.2:p.Ala66Val
ENST00000571307.1:n.563C>T
ENST00000571451.6:c.197C>T ENSP00000459661.2:p.Ala66Val
ENST00000572272.5:c.197C>T ENSP00000460475.1:p.Ala66Val
ENST00000577119.5:c.197C>T ENSP00000460216.1:p.Ala66Val
ENST00000613500.4:c.197C>T ENSP00000483359.1:p.Ala66Val
ENST00000617618.4:c.197C>T ENSP00000478516.1:p.Ala66Val
ENST00000619223.4:c.197C>T ENSP00000484692.1:p.Ala66Val
NM_001033053.2:c.197C>T NP_001028225.1:p.Ala66Val
NM_014922.4:c.197C>T NP_055737.1:p.Ala66Val
NM_033004.3:c.197C>T NP_127497.1:p.Ala66Val
NM_033006.3:c.197C>T NP_127499.1:p.Ala66Val
NM_033007.3:c.197C>T NP_127500.1:p.Ala66Val
NM_033004.4:c.197C>T MANE Select NP_127497.1:p.Ala66Val
NM_001033053.3:c.197C>T NP_001028225.1:p.Ala66Val
NM_014922.5:c.197C>T NP_055737.1:p.Ala66Val
NM_033006.4:c.197C>T NP_127499.1:p.Ala66Val
NM_033007.4:c.197C>T NP_127500.1:p.Ala66Val