Canonical Allele Identifier: CA2221840818
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722441_50722442delinsAC , CM000678.2:g.50722441_50722442delinsAC GRCh38
NC_000016.9:g.50756352_50756353delinsAC , CM000678.1:g.50756352_50756353delinsAC GRCh37
NC_000016.8:g.49313853_49313854delinsAC NCBI36
NG_007508.1:g.30303_30304delinsAC , LRG_177:g.30303_30304delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7377_2382-7376delinsAC ENSP00000493088.1:n.2382-7377_2382-7376delinsAC
ENST00000646677.2:c.*399-181_*399-180delinsAC ENSP00000496533.1:n.*399-181_*399-180delinsAC
ENST00000697425.1:c.461-181_461-180delinsAC
ENST00000697426.1:c.349-181_349-180delinsAC
ENST00000697427.1:c.265-181_265-180delinsAC
ENST00000697428.1:n.2112-181_2112-180delinsAC
ENST00000641284.1:c.2382-7377_2382-7376delinsAC ENSP00000493088.1:n.2382-7377_2382-7376delinsAC
ENST00000646677.1:c.*399-181_*399-180delinsAC ENSP00000496533.1:n.*399-181_*399-180delinsAC
ENST00000647318.2:c.2634-181_2634-180delinsAC MANE Select ENSP00000495993.1:n.2634-181_2634-180delinsAC
ENST00000300589.6:c.2715-181_2715-180delinsAC ENSP00000300589.2:n.2715-181_2715-180delinsAC
ENST00000524712.5:c.209-181_209-180delinsAC
ENST00000527052.5:c.181-181_181-180delinsAC
ENST00000529633.5:c.293-181_293-180delinsAC
ENST00000534057.1:c.349-181_349-180delinsAC
ENST00000534067.5:c.445-181_445-180delinsAC
NM_001293557.1:c.2634-181_2634-180delinsAC NP_001280486.1:n.2634-181_2634-180delinsAC
NM_022162.2:c.2715-181_2715-180delinsAC NP_071445.1:n.2715-181_2715-180delinsAC
XM_005256084.2:c.2634-181_2634-180delinsAC XP_005256141.1:n.2634-181_2634-180delinsAC
XM_006721242.2:c.2550-181_2550-180delinsAC XP_006721305.1:n.2550-181_2550-180delinsAC
XM_011523257.1:c.2211-181_2211-180delinsAC XP_011521559.1:n.2211-181_2211-180delinsAC
XM_011523258.1:c.2211-181_2211-180delinsAC XP_011521560.1:n.2211-181_2211-180delinsAC
XM_011523259.1:c.2049-181_2049-180delinsAC XP_011521561.1:n.2049-181_2049-180delinsAC
XR_429725.2:n.2556-181_2556-180delinsAC
XR_429726.2:n.2472-181_2472-180delinsAC
XR_933387.1:n.2752-181_2752-180delinsAC
XM_005256084.4:c.2634-181_2634-180delinsAC XP_005256141.1:n.2634-181_2634-180delinsAC
XM_006721242.4:c.2550-181_2550-180delinsAC XP_006721305.1:n.2550-181_2550-180delinsAC
XM_011523259.2:c.2049-181_2049-180delinsAC XP_011521561.1:n.2049-181_2049-180delinsAC
XM_017023535.1:c.2142-181_2142-180delinsAC XP_016879024.1:n.2142-181_2142-180delinsAC
XM_017023536.1:c.2049-181_2049-180delinsAC XP_016879025.1:n.2049-181_2049-180delinsAC
XM_017023537.1:c.2049-181_2049-180delinsAC XP_016879026.1:n.2049-181_2049-180delinsAC
XM_017023538.1:c.2049-181_2049-180delinsAC XP_016879027.1:n.2049-181_2049-180delinsAC
XR_429725.3:n.2509-181_2509-180delinsAC
XR_429726.3:n.2425-181_2425-180delinsAC
XR_933387.2:n.2705-181_2705-180delinsAC
NM_001293557.2:c.2634-181_2634-180delinsAC NP_001280486.1:n.2634-181_2634-180delinsAC
NM_001370466.1:c.2634-181_2634-180delinsAC MANE Select NP_001357395.1:n.2634-181_2634-180delinsAC
NM_022162.3:c.2715-181_2715-180delinsAC NP_071445.1:n.2715-181_2715-180delinsAC
NR_163434.1:n.2846-181_2846-180delinsAC