Canonical Allele Identifier: CA645546093
Gene: NOD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30452881_30452882del , CM000669.2:g.30452881_30452882del GRCh38
NC_000007.13:g.30492497_30492498del , CM000669.1:g.30492497_30492498del GRCh37
NC_000007.12:g.30459022_30459023del NCBI36
NG_013025.1:g.30896_30897del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222823.9:c.535_536del MANE Select ENSP00000222823.4:p.Ser179ProfsTer14
ENST00000222823.8:c.535_536del ENSP00000222823.4:p.Ser179ProfsTer14
ENST00000434755.5:c.535_536del ENSP00000416946.1:p.Ser179ProfsTer14
NM_006092.2:c.535_536del NP_006083.1:p.Ser179ProfsTer14
XM_005249568.1:c.535_536del XP_005249625.1:p.Ser179ProfsTer14
XM_005249572.1:c.535_536del XP_005249629.1:p.Ser179ProfsTer14
XM_005249576.1:c.-40_-39del XP_005249633.1:n.-40_-39del
XM_006715633.2:c.535_536del XP_006715696.1:p.Ser179ProfsTer14
XM_011515079.1:c.535_536del XP_011513381.1:p.Ser179ProfsTer14
XM_011515080.1:c.535_536del XP_011513382.1:p.Ser179ProfsTer14
XM_011515081.1:c.535_536del XP_011513383.1:p.Ser179ProfsTer14
XM_011515082.1:c.535_536del XP_011513384.1:p.Ser179ProfsTer14
XM_011515083.1:c.535_536del XP_011513385.1:p.Ser179ProfsTer14
XM_011515084.1:c.535_536del XP_011513386.1:p.Ser179ProfsTer14
XM_011515085.1:c.535_536del XP_011513387.1:p.Ser179ProfsTer14
XM_011515086.1:c.535_536del XP_011513388.1:p.Ser179ProfsTer14
XM_011515087.1:c.535_536del XP_011513389.1:p.Ser179ProfsTer14
XM_011515088.1:c.535_536del XP_011513390.1:p.Ser179ProfsTer14
XR_926907.1:n.1113_1114del
XR_926908.1:n.1113_1114del
XR_926909.1:n.1113_1114del
XR_926910.1:n.1113_1114del
NM_001354849.1:c.535_536del NP_001341778.1:p.Ser179ProfsTer14
NM_006092.3:c.535_536del NP_006083.1:p.Ser179ProfsTer14
NR_149002.1:n.1147_1148del
XM_011515080.2:c.535_536del XP_011513382.1:p.Ser179ProfsTer14
XM_011515081.2:c.535_536del XP_011513383.1:p.Ser179ProfsTer14
XM_011515088.2:c.535_536del XP_011513390.1:p.Ser179ProfsTer14
XM_017011674.1:c.535_536del XP_016867163.1:p.Ser179ProfsTer14
XR_001744529.1:n.1113_1114del
XR_001744530.1:n.1113_1114del
XR_002956406.1:n.1061_1062del
XR_926908.2:n.1113_1114del
XR_926909.2:n.1113_1114del
NM_006092.4:c.535_536del MANE Select NP_006083.1:p.Ser179ProfsTer14
NM_001354849.2:c.535_536del NP_001341778.1:p.Ser179ProfsTer14
NR_149002.2:n.1065_1066del