Canonical Allele Identifier: CA425461565

Gene: NLRC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32224713C>T , CM000664.2:g.32224713C>T	GRCh38
NC_000002.11:g.32449782C>T , CM000664.1:g.32449782C>T	GRCh37
NC_000002.10:g.32303286C>T	NCBI36
NG_041780.1:g.46031G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001199138.2:c.2835G>A MANE Select	NP_001186067.1:p.Ala945=
ENST00000402280.6:c.2835G>A MANE Select	ENSP00000385428.1:p.Ala945=
NM_001199138.1:c.2835G>A	NP_001186067.1:p.Ala945=
NM_001199139.1:c.2835G>A	NP_001186068.1:p.Ala945=
NM_001302504.1:c.840G>A	NP_001289433.1:p.Ala280=
NM_021209.4:c.2835G>A	NP_067032.3:p.Ala945=
ENST00000342905.10:c.840G>A	ENSP00000339666.6:p.Ala280=
ENST00000360906.9:c.2835G>A	ENSP00000354159.5:p.Ala945=
ENST00000402280.5:c.2835G>A	ENSP00000385428.1:p.Ala945=
ENST00000404025.2:c.2835G>A	ENSP00000385090.2:p.Ala945=
ENST00000404025.3:c.*541G>A	ENSP00000385090.3:n.*541G>A
ENST00000652197.1:c.*565G>A	ENSP00000498301.1:n.*565G>A
ENST00000652197.2:c.528G>A	ENSP00000498301.2:p.Ala176=