Canonical Allele Identifier: CA2658534427

Gene: NLRC4

Linked Data

• gnomAD v4: 2-32251281-TCAGAGCCTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32251284_32251293del , CM000664.2:g.32251284_32251293del	GRCh38
NC_000002.11:g.32476353_32476362del , CM000664.1:g.32476353_32476362del	GRCh37
NC_000002.10:g.32329857_32329866del	NCBI36
NG_041780.1:g.19453_19462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652197.2:c.-76+5484_-76+5493del	ENSP00000498301.2:n.-76+5484_-76+5493del
ENST00000402280.6:c.573_582del MANE Select	ENSP00000385428.1:p.Cys191Ter
ENST00000404025.3:c.573_582del	ENSP00000385090.3:p.Cys191Ter
ENST00000652197.1:c.573_582del	ENSP00000498301.1:p.Cys191Ter
ENST00000342905.10:c.262+1128_262+1137del	ENSP00000339666.6:n.262+1128_262+1137del
ENST00000360906.9:c.573_582del	ENSP00000354159.5:p.Cys191Ter
ENST00000402280.5:c.573_582del	ENSP00000385428.1:p.Cys191Ter
ENST00000404025.2:c.573_582del	ENSP00000385090.2:p.Cys191Ter
NM_001199138.1:c.573_582del	NP_001186067.1:p.Cys191Ter
NM_001199139.1:c.573_582del	NP_001186068.1:p.Cys191Ter
NM_001302504.1:c.262+1128_262+1137del	NP_001289433.1:n.262+1128_262+1137del
NM_021209.4:c.573_582del	NP_067032.3:p.Cys191Ter
XM_011533008.1:c.573_582del	XP_011531310.1:p.Cys191Ter
XM_017004619.1:c.573_582del	XP_016860108.1:p.Cys191Ter
XR_001738872.1:n.834_843del
NM_001199138.2:c.573_582del MANE Select	NP_001186067.1:p.Cys191Ter