Canonical Allele Identifier: CA573759997
Gene: NOD1 HGNC NCBI

Linked Data

dbSNP Id: rs1353927855

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30452952_30452953del , CM000669.2:g.30452952_30452953del GRCh38
NC_000007.13:g.30492568_30492569del , CM000669.1:g.30492568_30492569del GRCh37
NC_000007.12:g.30459093_30459094del NCBI36
NG_013025.1:g.30825_30826del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222823.9:c.464_465del MANE Select ENSP00000222823.4:p.Leu155ArgfsTer17
ENST00000222823.8:c.464_465del ENSP00000222823.4:p.Leu155ArgfsTer17
ENST00000434755.5:c.464_465del ENSP00000416946.1:p.Leu155ArgfsTer17
NM_006092.2:c.464_465del NP_006083.1:p.Leu155ArgfsTer17
XM_005249568.1:c.464_465del XP_005249625.1:p.Leu155ArgfsTer17
XM_005249572.1:c.464_465del XP_005249629.1:p.Leu155ArgfsTer17
XM_006715633.2:c.464_465del XP_006715696.1:p.Leu155ArgfsTer17
XM_011515079.1:c.464_465del XP_011513381.1:p.Leu155ArgfsTer17
XM_011515080.1:c.464_465del XP_011513382.1:p.Leu155ArgfsTer17
XM_011515081.1:c.464_465del XP_011513383.1:p.Leu155ArgfsTer17
XM_011515082.1:c.464_465del XP_011513384.1:p.Leu155ArgfsTer17
XM_011515083.1:c.464_465del XP_011513385.1:p.Leu155ArgfsTer17
XM_011515084.1:c.464_465del XP_011513386.1:p.Leu155ArgfsTer17
XM_011515085.1:c.464_465del XP_011513387.1:p.Leu155ArgfsTer17
XM_011515086.1:c.464_465del XP_011513388.1:p.Leu155ArgfsTer17
XM_011515087.1:c.464_465del XP_011513389.1:p.Leu155ArgfsTer17
XM_011515088.1:c.464_465del XP_011513390.1:p.Leu155ArgfsTer17
XR_926907.1:n.1042_1043del
XR_926908.1:n.1042_1043del
XR_926909.1:n.1042_1043del
XR_926910.1:n.1042_1043del
NM_001354849.1:c.464_465del NP_001341778.1:p.Leu155ArgfsTer17
NM_006092.3:c.464_465del NP_006083.1:p.Leu155ArgfsTer17
NR_149002.1:n.1076_1077del
XM_011515080.2:c.464_465del XP_011513382.1:p.Leu155ArgfsTer17
XM_011515081.2:c.464_465del XP_011513383.1:p.Leu155ArgfsTer17
XM_011515088.2:c.464_465del XP_011513390.1:p.Leu155ArgfsTer17
XM_017011674.1:c.464_465del XP_016867163.1:p.Leu155ArgfsTer17
XR_001744529.1:n.1042_1043del
XR_001744530.1:n.1042_1043del
XR_002956406.1:n.990_991del
XR_926908.2:n.1042_1043del
XR_926909.2:n.1042_1043del
NM_006092.4:c.464_465del MANE Select NP_006083.1:p.Leu155ArgfsTer17
NM_001354849.2:c.464_465del NP_001341778.1:p.Leu155ArgfsTer17
NR_149002.2:n.994_995del