Canonical Allele Identifier: CA2221842561
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50723083_50723084delinsGC , CM000678.2:g.50723083_50723084delinsGC GRCh38
NC_000016.9:g.50756994_50756995delinsGC , CM000678.1:g.50756994_50756995delinsGC GRCh37
NC_000016.8:g.49314495_49314496delinsGC NCBI36
NG_007508.1:g.30945_30946delinsGC , LRG_177:g.30945_30946delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.2382-6735_2382-6734delinsGC ENSP00000493088.1:n.2382-6735_2382-6734delinsGC
ENST00000646677.2:c.*483-218_*483-217delinsGC ENSP00000496533.1:n.*483-218_*483-217delinsGC
ENST00000697425.1:c.545-218_545-217delinsGC
ENST00000697426.1:c.433-218_433-217delinsGC
ENST00000697427.1:c.349-218_349-217delinsGC
ENST00000697428.1:n.2196-218_2196-217delinsGC
ENST00000641284.1:c.2382-6735_2382-6734delinsGC ENSP00000493088.1:n.2382-6735_2382-6734delinsGC
ENST00000646677.1:c.*483-218_*483-217delinsGC ENSP00000496533.1:n.*483-218_*483-217delinsGC
ENST00000647318.2:c.2718-218_2718-217delinsGC MANE Select ENSP00000495993.1:n.2718-218_2718-217delinsGC
ENST00000300589.6:c.2799-218_2799-217delinsGC ENSP00000300589.2:n.2799-218_2799-217delinsGC
ENST00000524712.5:c.293-218_293-217delinsGC
ENST00000527052.5:c.265-218_265-217delinsGC
ENST00000529633.5:c.377-218_377-217delinsGC
ENST00000534057.1:c.433-218_433-217delinsGC
ENST00000534067.5:c.529-218_529-217delinsGC
NM_001293557.1:c.2718-218_2718-217delinsGC NP_001280486.1:n.2718-218_2718-217delinsGC
NM_022162.2:c.2799-218_2799-217delinsGC NP_071445.1:n.2799-218_2799-217delinsGC
XM_005256084.2:c.2718-218_2718-217delinsGC XP_005256141.1:n.2718-218_2718-217delinsGC
XM_006721242.2:c.2634-218_2634-217delinsGC XP_006721305.1:n.2634-218_2634-217delinsGC
XM_011523257.1:c.2295-218_2295-217delinsGC XP_011521559.1:n.2295-218_2295-217delinsGC
XM_011523258.1:c.2295-218_2295-217delinsGC XP_011521560.1:n.2295-218_2295-217delinsGC
XM_011523259.1:c.2133-218_2133-217delinsGC XP_011521561.1:n.2133-218_2133-217delinsGC
XR_429725.2:n.2640-218_2640-217delinsGC
XR_429726.2:n.2556-218_2556-217delinsGC
XR_933387.1:n.2836-218_2836-217delinsGC
XM_005256084.4:c.2718-218_2718-217delinsGC XP_005256141.1:n.2718-218_2718-217delinsGC
XM_006721242.4:c.2634-218_2634-217delinsGC XP_006721305.1:n.2634-218_2634-217delinsGC
XM_011523259.2:c.2133-218_2133-217delinsGC XP_011521561.1:n.2133-218_2133-217delinsGC
XM_017023535.1:c.2226-218_2226-217delinsGC XP_016879024.1:n.2226-218_2226-217delinsGC
XM_017023536.1:c.2133-218_2133-217delinsGC XP_016879025.1:n.2133-218_2133-217delinsGC
XM_017023537.1:c.2133-218_2133-217delinsGC XP_016879026.1:n.2133-218_2133-217delinsGC
XM_017023538.1:c.2133-218_2133-217delinsGC XP_016879027.1:n.2133-218_2133-217delinsGC
XR_429725.3:n.2593-218_2593-217delinsGC
XR_429726.3:n.2509-218_2509-217delinsGC
XR_933387.2:n.2789-218_2789-217delinsGC
NM_001293557.2:c.2718-218_2718-217delinsGC NP_001280486.1:n.2718-218_2718-217delinsGC
NM_001370466.1:c.2718-218_2718-217delinsGC MANE Select NP_001357395.1:n.2718-218_2718-217delinsGC
NM_022162.3:c.2799-218_2799-217delinsGC NP_071445.1:n.2799-218_2799-217delinsGC
NR_163434.1:n.2930-218_2930-217delinsGC