Canonical Allele Identifier: CA1242559202

Gene: NLRC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32251267G= , CM000664.2:g.32251267G=	GRCh38
NC_000002.11:g.32476336G= , CM000664.1:g.32476336G=	GRCh37
NC_000002.10:g.32329840G=	NCBI36
NG_041780.1:g.19477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652197.2:c.-76+5508C=	ENSP00000498301.2:n.-76+5508C=
ENST00000402280.6:c.597C= MANE Select	ENSP00000385428.1:p.Phe199=
ENST00000404025.3:c.597C=	ENSP00000385090.3:p.Phe199=
ENST00000652197.1:c.597C=	ENSP00000498301.1:p.Phe199=
ENST00000342905.10:c.262+1152C=	ENSP00000339666.6:n.262+1152C=
ENST00000360906.9:c.597C=	ENSP00000354159.5:p.Phe199=
ENST00000402280.5:c.597C=	ENSP00000385428.1:p.Phe199=
ENST00000404025.2:c.597C=	ENSP00000385090.2:p.Phe199=
NM_001199138.1:c.597C=	NP_001186067.1:p.Phe199=
NM_001199139.1:c.597C=	NP_001186068.1:p.Phe199=
NM_001302504.1:c.262+1152C=	NP_001289433.1:n.262+1152C=
NM_021209.4:c.597C=	NP_067032.3:p.Phe199=
XM_011533008.1:c.597C=	XP_011531310.1:p.Phe199=
XM_017004619.1:c.597C=	XP_016860108.1:p.Phe199=
XR_001738872.1:n.858C=
NM_001199138.2:c.597C= MANE Select	NP_001186067.1:p.Phe199=