Canonical Allele Identifier: CA346514384

Gene: NLRC4

Linked Data

• gnomAD v4: 2-32251083-T-C
• MyVariant Identifiers: chr2:g.32476152T>C (hg19) ; chr2:g.32251083T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32251083T>C , CM000664.2:g.32251083T>C	GRCh38
NC_000002.11:g.32476152T>C , CM000664.1:g.32476152T>C	GRCh37
NC_000002.10:g.32329656T>C	NCBI36
NG_041780.1:g.19661A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652197.2:c.-76+5692A>G	ENSP00000498301.2:n.-76+5692A>G
ENST00000402280.6:c.781A>G MANE Select	ENSP00000385428.1:p.Ile261Val
ENST00000404025.3:c.781A>G	ENSP00000385090.3:p.Ile261Val
ENST00000652197.1:c.781A>G	ENSP00000498301.1:p.Ile261Val
ENST00000342905.10:c.262+1336A>G	ENSP00000339666.6:n.262+1336A>G
ENST00000360906.9:c.781A>G	ENSP00000354159.5:p.Ile261Val
ENST00000402280.5:c.781A>G	ENSP00000385428.1:p.Ile261Val
ENST00000404025.2:c.781A>G	ENSP00000385090.2:p.Ile261Val
NM_001199138.1:c.781A>G	NP_001186067.1:p.Ile261Val
NM_001199139.1:c.781A>G	NP_001186068.1:p.Ile261Val
NM_001302504.1:c.262+1336A>G	NP_001289433.1:n.262+1336A>G
NM_021209.4:c.781A>G	NP_067032.3:p.Ile261Val
XM_011533008.1:c.781A>G	XP_011531310.1:p.Ile261Val
XM_017004619.1:c.781A>G	XP_016860108.1:p.Ile261Val
XR_001738872.1:n.1042A>G
NM_001199138.2:c.781A>G MANE Select	NP_001186067.1:p.Ile261Val