Canonical Allele Identifier: CA1697735459
Gene: NOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30452203C= , CM000669.2:g.30452203C= GRCh38
NC_000007.13:g.30491819C= , CM000669.1:g.30491819C= GRCh37
NC_000007.12:g.30458344C= NCBI36
NG_013025.1:g.31575G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222823.9:c.1214G= MANE Select ENSP00000222823.4:p.Arg405=
ENST00000222823.8:c.1214G= ENSP00000222823.4:p.Arg405=
ENST00000434755.5:c.1214G= ENSP00000416946.1:p.Arg405=
NM_006092.2:c.1214G= NP_006083.1:p.Arg405=
XM_005249568.1:c.1214G= XP_005249625.1:p.Arg405=
XM_005249572.1:c.1214G= XP_005249629.1:p.Arg405=
XM_005249576.1:c.470G= XP_005249633.1:p.Arg157=
XM_006715633.2:c.1214G= XP_006715696.1:p.Arg405=
XM_011515079.1:c.1214G= XP_011513381.1:p.Arg405=
XM_011515080.1:c.1214G= XP_011513382.1:p.Arg405=
XM_011515081.1:c.1214G= XP_011513383.1:p.Arg405=
XM_011515082.1:c.1214G= XP_011513384.1:p.Arg405=
XM_011515083.1:c.1214G= XP_011513385.1:p.Arg405=
XM_011515084.1:c.1214G= XP_011513386.1:p.Arg405=
XM_011515085.1:c.1214G= XP_011513387.1:p.Arg405=
XM_011515086.1:c.1214G= XP_011513388.1:p.Arg405=
XM_011515087.1:c.1214G= XP_011513389.1:p.Arg405=
XM_011515088.1:c.1214G= XP_011513390.1:p.Arg405=
XR_926907.1:n.1792G=
XR_926908.1:n.1792G=
XR_926909.1:n.1792G=
XR_926910.1:n.1792G=
NM_001354849.1:c.1214G= NP_001341778.1:p.Arg405=
NM_006092.3:c.1214G= NP_006083.1:p.Arg405=
NR_149002.1:n.1826G=
XM_011515080.2:c.1214G= XP_011513382.1:p.Arg405=
XM_011515081.2:c.1214G= XP_011513383.1:p.Arg405=
XM_011515088.2:c.1214G= XP_011513390.1:p.Arg405=
XM_017011674.1:c.1214G= XP_016867163.1:p.Arg405=
XR_001744529.1:n.1792G=
XR_001744530.1:n.1792G=
XR_002956406.1:n.1740G=
XR_926908.2:n.1792G=
XR_926909.2:n.1792G=
NM_006092.4:c.1214G= MANE Select NP_006083.1:p.Arg405=
NM_001354849.2:c.1214G= NP_001341778.1:p.Arg405=
NR_149002.2:n.1744G=