Canonical Allele Identifier: CA1601734

Gene: NLRC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32235536C>T , CM000664.2:g.32235536C>T	GRCh38
NC_000002.11:g.32460605C>T , CM000664.1:g.32460605C>T	GRCh37
NC_000002.10:g.32314109C>T	NCBI36
NG_041780.1:g.35208G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001199138.2:c.2647G>A MANE Select	NP_001186067.1:p.Ala883Thr
ENST00000402280.6:c.2647G>A MANE Select	ENSP00000385428.1:p.Ala883Thr
NM_001199138.1:c.2647G>A	NP_001186067.1:p.Ala883Thr
NM_001199139.1:c.2647G>A	NP_001186068.1:p.Ala883Thr
NM_001302504.1:c.652G>A	NP_001289433.1:p.Ala218Thr
NM_021209.4:c.2647G>A	NP_067032.3:p.Ala883Thr
ENST00000342905.10:c.652G>A	ENSP00000339666.6:p.Ala218Thr
ENST00000360906.9:c.2647G>A	ENSP00000354159.5:p.Ala883Thr
ENST00000402280.5:c.2647G>A	ENSP00000385428.1:p.Ala883Thr
ENST00000404025.2:c.2647G>A	ENSP00000385090.2:p.Ala883Thr
ENST00000404025.3:c.*353G>A	ENSP00000385090.3:n.*353G>A
ENST00000652197.1:c.*377G>A	ENSP00000498301.1:n.*377G>A
ENST00000652197.2:c.340G>A	ENSP00000498301.2:p.Ala114Thr
XR_001738872.1:n.2913G>A