Canonical Allele Identifier: CA2633164440
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50723155_50723159del , CM000678.2:g.50723155_50723159del GRCh38
NC_000016.9:g.50757066_50757070del , CM000678.1:g.50757066_50757070del GRCh37
NC_000016.8:g.49314567_49314571del NCBI36
NG_007508.1:g.31017_31021del , LRG_177:g.31017_31021del

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-6663_2382-6659del ENSP00000493088.1:n.2382-6663_2382-6659del
ENST00000646677.2:c.*483-146_*483-142del ENSP00000496533.1:n.*483-146_*483-142del
ENST00000697425.1:c.545-146_545-142del
ENST00000697426.1:c.433-146_433-142del
ENST00000697427.1:c.349-146_349-142del
ENST00000697428.1:n.2196-146_2196-142del
ENST00000641284.1:c.2382-6663_2382-6659del ENSP00000493088.1:n.2382-6663_2382-6659del
ENST00000646677.1:c.*483-146_*483-142del ENSP00000496533.1:n.*483-146_*483-142del
ENST00000647318.2:c.2718-146_2718-142del MANE Select ENSP00000495993.1:n.2718-146_2718-142del
ENST00000300589.6:c.2799-146_2799-142del ENSP00000300589.2:n.2799-146_2799-142del
ENST00000524712.5:c.293-146_293-142del
ENST00000527052.5:c.265-146_265-142del
ENST00000529633.5:c.377-146_377-142del
ENST00000534057.1:c.433-146_433-142del
ENST00000534067.5:c.529-146_529-142del
NM_001293557.1:c.2718-146_2718-142del NP_001280486.1:n.2718-146_2718-142del
NM_022162.2:c.2799-146_2799-142del NP_071445.1:n.2799-146_2799-142del
XM_005256084.2:c.2718-146_2718-142del XP_005256141.1:n.2718-146_2718-142del
XM_006721242.2:c.2634-146_2634-142del XP_006721305.1:n.2634-146_2634-142del
XM_011523257.1:c.2295-146_2295-142del XP_011521559.1:n.2295-146_2295-142del
XM_011523258.1:c.2295-146_2295-142del XP_011521560.1:n.2295-146_2295-142del
XM_011523259.1:c.2133-146_2133-142del XP_011521561.1:n.2133-146_2133-142del
XR_429725.2:n.2640-146_2640-142del
XR_429726.2:n.2556-146_2556-142del
XR_933387.1:n.2836-146_2836-142del
XM_005256084.4:c.2718-146_2718-142del XP_005256141.1:n.2718-146_2718-142del
XM_006721242.4:c.2634-146_2634-142del XP_006721305.1:n.2634-146_2634-142del
XM_011523259.2:c.2133-146_2133-142del XP_011521561.1:n.2133-146_2133-142del
XM_017023535.1:c.2226-146_2226-142del XP_016879024.1:n.2226-146_2226-142del
XM_017023536.1:c.2133-146_2133-142del XP_016879025.1:n.2133-146_2133-142del
XM_017023537.1:c.2133-146_2133-142del XP_016879026.1:n.2133-146_2133-142del
XM_017023538.1:c.2133-146_2133-142del XP_016879027.1:n.2133-146_2133-142del
XR_429725.3:n.2593-146_2593-142del
XR_429726.3:n.2509-146_2509-142del
XR_933387.2:n.2789-146_2789-142del
NM_001293557.2:c.2718-146_2718-142del NP_001280486.1:n.2718-146_2718-142del
NM_001370466.1:c.2718-146_2718-142del MANE Select NP_001357395.1:n.2718-146_2718-142del
NM_022162.3:c.2799-146_2799-142del NP_071445.1:n.2799-146_2799-142del
NR_163434.1:n.2930-146_2930-142del