Canonical Allele Identifier: CA425621798

Gene: NLRC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32250700C>G , CM000664.2:g.32250700C>G	GRCh38
NC_000002.11:g.32475769C>G , CM000664.1:g.32475769C>G	GRCh37
NC_000002.10:g.32329273C>G	NCBI36
NG_041780.1:g.20044G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001199138.2:c.1164G>C MANE Select	NP_001186067.1:p.Arg388=
ENST00000402280.6:c.1164G>C MANE Select	ENSP00000385428.1:p.Arg388=
NM_001199138.1:c.1164G>C	NP_001186067.1:p.Arg388=
NM_001199139.1:c.1164G>C	NP_001186068.1:p.Arg388=
NM_001302504.1:c.262+1719G>C	NP_001289433.1:n.262+1719G>C
NM_021209.4:c.1164G>C	NP_067032.3:p.Arg388=
ENST00000342905.10:c.262+1719G>C	ENSP00000339666.6:n.262+1719G>C
ENST00000360906.9:c.1164G>C	ENSP00000354159.5:p.Arg388=
ENST00000402280.5:c.1164G>C	ENSP00000385428.1:p.Arg388=
ENST00000404025.2:c.1164G>C	ENSP00000385090.2:p.Arg388=
ENST00000404025.3:c.1164G>C	ENSP00000385090.3:p.Arg388=
ENST00000652197.1:c.1164G>C	ENSP00000498301.1:p.Arg388=
ENST00000652197.2:c.-76+6075G>C	ENSP00000498301.2:n.-76+6075G>C
XM_011533008.1:c.1164G>C	XP_011531310.1:p.Arg388=
XM_017004619.1:c.1164G>C	XP_016860108.1:p.Arg388=
XR_001738872.1:n.1425G>C