Canonical Allele Identifier: CA1602133

Gene: NLRC4

Linked Data

• dbSNP Id: rs750839705
• ExAC: 2:32476431 C / CCTGGGCCCTGCTGAGACGGAGGAAG
• MyVariant Identifiers: chr2:g.32476431_32476432insCTGGGCCCTGCTGAGACGGAGGAAG (hg19) ; chr2:g.32251362_32251363insCTGGGCCCTGCTGAGACGGAGGAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32251362_32251363insCTGGGCCCTGCTGAGACGGAGGAAG , CM000664.2:g.32251362_32251363insCTGGGCCCTGCTGAGACGGAGGAAG	GRCh38
NC_000002.11:g.32476431_32476432insCTGGGCCCTGCTGAGACGGAGGAAG , CM000664.1:g.32476431_32476432insCTGGGCCCTGCTGAGACGGAGGAAG	GRCh37
NC_000002.10:g.32329935_32329936insCTGGGCCCTGCTGAGACGGAGGAAG	NCBI36
NG_041780.1:g.19381_19382insCTTCCTCCGTCTCAGCAGGGCCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652197.2:c.-76+5412_-76+5413insCTTCCTCCGTCTCAGCAGGGCCCAG	ENSP00000498301.2:n.-76+5412_-76+5413insCTTCCTCCGTCTCAGCAGGGC...
ENST00000402280.6:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG MANE Select	ENSP00000385428.1:p.Glu168LeufsTer?
ENST00000404025.3:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	ENSP00000385090.3:p.Glu168LeufsTer?
ENST00000652197.1:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	ENSP00000498301.1:p.Glu168LeufsTer?
ENST00000342905.10:c.262+1056_262+1057insCTTCCTCCGTCTCAGCAGGGCCCAG	ENSP00000339666.6:n.262+1056_262+1057insCTTCCTCCGTCTCAGCAGGGC...
ENST00000360906.9:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	ENSP00000354159.5:p.Glu168LeufsTer?
ENST00000402280.5:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	ENSP00000385428.1:p.Glu168LeufsTer?
ENST00000404025.2:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	ENSP00000385090.2:p.Glu168LeufsTer?
NM_001199138.1:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	NP_001186067.1:p.Glu168LeufsTer?
NM_001199139.1:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	NP_001186068.1:p.Glu168LeufsTer?
NM_001302504.1:c.262+1056_262+1057insCTTCCTCCGTCTCAGCAGGGCCCAG	NP_001289433.1:n.262+1056_262+1057insCTTCCTCCGTCTCAGCAGGGCCCA...
NM_021209.4:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	NP_067032.3:p.Glu168LeufsTer?
XM_011533008.1:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	XP_011531310.1:p.Glu168LeufsTer?
XM_017004619.1:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG	XP_016860108.1:p.Glu168LeufsTer?
XR_001738872.1:n.762_763insCTTCCTCCGTCTCAGCAGGGCCCAG
NM_001199138.2:c.501_502insCTTCCTCCGTCTCAGCAGGGCCCAG MANE Select	NP_001186067.1:p.Glu168LeufsTer?