Canonical Allele Identifier: CA1099835381
Gene: NOD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30452960_30452964del , CM000669.2:g.30452960_30452964del GRCh38
NC_000007.13:g.30492576_30492580del , CM000669.1:g.30492576_30492580del GRCh37
NC_000007.12:g.30459101_30459105del NCBI36
NG_013025.1:g.30814_30818del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222823.9:c.453_457del MANE Select ENSP00000222823.4:p.Glu151AspfsTer20
ENST00000222823.8:c.453_457del ENSP00000222823.4:p.Glu151AspfsTer20
ENST00000434755.5:c.453_457del ENSP00000416946.1:p.Glu151AspfsTer20
NM_006092.2:c.453_457del NP_006083.1:p.Glu151AspfsTer20
XM_005249568.1:c.453_457del XP_005249625.1:p.Glu151AspfsTer20
XM_005249572.1:c.453_457del XP_005249629.1:p.Glu151AspfsTer20
XM_006715633.2:c.453_457del XP_006715696.1:p.Glu151AspfsTer20
XM_011515079.1:c.453_457del XP_011513381.1:p.Glu151AspfsTer20
XM_011515080.1:c.453_457del XP_011513382.1:p.Glu151AspfsTer20
XM_011515081.1:c.453_457del XP_011513383.1:p.Glu151AspfsTer20
XM_011515082.1:c.453_457del XP_011513384.1:p.Glu151AspfsTer20
XM_011515083.1:c.453_457del XP_011513385.1:p.Glu151AspfsTer20
XM_011515084.1:c.453_457del XP_011513386.1:p.Glu151AspfsTer20
XM_011515085.1:c.453_457del XP_011513387.1:p.Glu151AspfsTer20
XM_011515086.1:c.453_457del XP_011513388.1:p.Glu151AspfsTer20
XM_011515087.1:c.453_457del XP_011513389.1:p.Glu151AspfsTer20
XM_011515088.1:c.453_457del XP_011513390.1:p.Glu151AspfsTer20
XR_926907.1:n.1031_1035del
XR_926908.1:n.1031_1035del
XR_926909.1:n.1031_1035del
XR_926910.1:n.1031_1035del
NM_001354849.1:c.453_457del NP_001341778.1:p.Glu151AspfsTer20
NM_006092.3:c.453_457del NP_006083.1:p.Glu151AspfsTer20
NR_149002.1:n.1065_1069del
XM_011515080.2:c.453_457del XP_011513382.1:p.Glu151AspfsTer20
XM_011515081.2:c.453_457del XP_011513383.1:p.Glu151AspfsTer20
XM_011515088.2:c.453_457del XP_011513390.1:p.Glu151AspfsTer20
XM_017011674.1:c.453_457del XP_016867163.1:p.Glu151AspfsTer20
XR_001744529.1:n.1031_1035del
XR_001744530.1:n.1031_1035del
XR_002956406.1:n.979_983del
XR_926908.2:n.1031_1035del
XR_926909.2:n.1031_1035del
NM_006092.4:c.453_457del MANE Select NP_006083.1:p.Glu151AspfsTer20
NM_001354849.2:c.453_457del NP_001341778.1:p.Glu151AspfsTer20
NR_149002.2:n.983_987del