Canonical Allele Identifier: CA1242559241

Gene: NLRC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32251362_32251369delinsCAATGATG , CM000664.2:g.32251362_32251369delinsCAATGATG	GRCh38
NC_000002.11:g.32476431_32476438delinsCAATGATG , CM000664.1:g.32476431_32476438delinsCAATGATG	GRCh37
NC_000002.10:g.32329935_32329942delinsCAATGATG	NCBI36
NG_041780.1:g.19375_19382delinsCATCATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652197.2:c.-76+5406_-76+5413delinsCATCATTG	ENSP00000498301.2:n.-76+5406_-76+5413delinsCATCATTG
ENST00000402280.6:c.495_502delinsCATCATTG MANE Select	ENSP00000385428.1:p.Cys165=
ENST00000404025.3:c.495_502delinsCATCATTG	ENSP00000385090.3:p.Cys165=
ENST00000652197.1:c.495_502delinsCATCATTG	ENSP00000498301.1:p.Cys165=
ENST00000342905.10:c.262+1050_262+1057delinsCATCATTG	ENSP00000339666.6:n.262+1050_262+1057delinsCATCATTG
ENST00000360906.9:c.495_502delinsCATCATTG	ENSP00000354159.5:p.Cys165=
ENST00000402280.5:c.495_502delinsCATCATTG	ENSP00000385428.1:p.Cys165=
ENST00000404025.2:c.495_502delinsCATCATTG	ENSP00000385090.2:p.Cys165=
NM_001199138.1:c.495_502delinsCATCATTG	NP_001186067.1:p.Cys165=
NM_001199139.1:c.495_502delinsCATCATTG	NP_001186068.1:p.Cys165=
NM_001302504.1:c.262+1050_262+1057delinsCATCATTG	NP_001289433.1:n.262+1050_262+1057delinsCATCATTG
NM_021209.4:c.495_502delinsCATCATTG	NP_067032.3:p.Cys165=
XM_011533008.1:c.495_502delinsCATCATTG	XP_011531310.1:p.Cys165=
XM_017004619.1:c.495_502delinsCATCATTG	XP_016860108.1:p.Cys165=
XR_001738872.1:n.756_763delinsCATCATTG
NM_001199138.2:c.495_502delinsCATCATTG MANE Select	NP_001186067.1:p.Cys165=