Canonical Allele Identifier: CA346519587
Gene: NLRC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32224746G>T , CM000664.2:g.32224746G>T GRCh38
NC_000002.11:g.32449815G>T , CM000664.1:g.32449815G>T GRCh37
NC_000002.10:g.32303319G>T NCBI36
NG_041780.1:g.45998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652197.2:c.495C>A ENSP00000498301.2:p.Asn165Lys
ENST00000402280.6:c.2802C>A MANE Select ENSP00000385428.1:p.Asn934Lys
ENST00000404025.3:c.*508C>A ENSP00000385090.3:n.*508C>A
ENST00000652197.1:c.*532C>A ENSP00000498301.1:n.*532C>A
ENST00000342905.10:c.807C>A ENSP00000339666.6:p.Asn269Lys
ENST00000360906.9:c.2802C>A ENSP00000354159.5:p.Asn934Lys
ENST00000402280.5:c.2802C>A ENSP00000385428.1:p.Asn934Lys
ENST00000404025.2:c.2802C>A ENSP00000385090.2:p.Asn934Lys
NM_001199138.1:c.2802C>A NP_001186067.1:p.Asn934Lys
NM_001199139.1:c.2802C>A NP_001186068.1:p.Asn934Lys
NM_001302504.1:c.807C>A NP_001289433.1:p.Asn269Lys
NM_021209.4:c.2802C>A NP_067032.3:p.Asn934Lys
XR_001738872.1:n.3068C>A
NM_001199138.2:c.2802C>A MANE Select NP_001186067.1:p.Asn934Lys