Canonical Allele Identifier: CA1697736203
Gene: NOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30452425_30452446delinsGTGAGCAGCTTGCTAGCCCCCT , CM000669.2:g.30452425_30452446delinsGTGAGCAGCTTGCTAGCCCCCT GRCh38
NC_000007.13:g.30492041_30492062delinsGTGAGCAGCTTGCTAGCCCCCT , CM000669.1:g.30492041_30492062delinsGTGAGCAGCTTGCTAGCCCCCT GRCh37
NC_000007.12:g.30458566_30458587delinsGTGAGCAGCTTGCTAGCCCCCT NCBI36
NG_013025.1:g.31332_31353delinsAGGGGGCTAGCAAGCTGCTCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000222823.9:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC MANE Select ENSP00000222823.4:p.Lys324=
ENST00000222823.8:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC ENSP00000222823.4:p.Lys324=
ENST00000434755.5:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC ENSP00000416946.1:p.Lys324=
NM_006092.2:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC NP_006083.1:p.Lys324=
XM_005249568.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_005249625.1:p.Lys324=
XM_005249572.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_005249629.1:p.Lys324=
XM_005249576.1:c.227_248delinsAGGGGGCTAGCAAGCTGCTCAC XP_005249633.1:p.Lys76=
XM_006715633.2:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_006715696.1:p.Lys324=
XM_011515079.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513381.1:p.Lys324=
XM_011515080.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513382.1:p.Lys324=
XM_011515081.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513383.1:p.Lys324=
XM_011515082.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513384.1:p.Lys324=
XM_011515083.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513385.1:p.Lys324=
XM_011515084.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513386.1:p.Lys324=
XM_011515085.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513387.1:p.Lys324=
XM_011515086.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513388.1:p.Lys324=
XM_011515087.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513389.1:p.Lys324=
XM_011515088.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513390.1:p.Lys324=
XR_926907.1:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
XR_926908.1:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
XR_926909.1:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
XR_926910.1:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
NM_001354849.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC NP_001341778.1:p.Lys324=
NM_006092.3:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC NP_006083.1:p.Lys324=
NR_149002.1:n.1583_1604delinsAGGGGGCTAGCAAGCTGCTCAC
XM_011515080.2:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513382.1:p.Lys324=
XM_011515081.2:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513383.1:p.Lys324=
XM_011515088.2:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_011513390.1:p.Lys324=
XM_017011674.1:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC XP_016867163.1:p.Lys324=
XR_001744529.1:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
XR_001744530.1:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
XR_002956406.1:n.1497_1518delinsAGGGGGCTAGCAAGCTGCTCAC
XR_926908.2:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
XR_926909.2:n.1549_1570delinsAGGGGGCTAGCAAGCTGCTCAC
NM_006092.4:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC MANE Select NP_006083.1:p.Lys324=
NM_001354849.2:c.971_992delinsAGGGGGCTAGCAAGCTGCTCAC NP_001341778.1:p.Lys324=
NR_149002.2:n.1501_1522delinsAGGGGGCTAGCAAGCTGCTCAC