Canonical Allele Identifier: CA2221849940
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50705694_50705696delinsCTT , CM000678.2:g.50705694_50705696delinsCTT GRCh38
NC_000016.9:g.50739605_50739607delinsCTT , CM000678.1:g.50739605_50739607delinsCTT GRCh37
NC_000016.8:g.49297106_49297108delinsCTT NCBI36
NG_007508.1:g.13556_13558delinsCTT , LRG_177:g.13556_13558delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.460-2161_460-2159delinsCTT ENSP00000493088.1:n.460-2161_460-2159deli...
ENST00000646677.2:c.460-2161_460-2159delinsCTT ENSP00000496533.1:n.460-2161_460-2159deli...
ENST00000641284.1:c.460-2161_460-2159delinsCTT ENSP00000493088.1:n.460-2161_460-2159deli...
ENST00000646677.1:c.460-2161_460-2159delinsCTT ENSP00000496533.1:n.460-2161_460-2159deli...
ENST00000647318.2:c.460-2161_460-2159delinsCTT MANE Select ENSP00000495993.1:n.460-2161_460-2159deli...
ENST00000300589.6:c.541-2161_541-2159delinsCTT ENSP00000300589.2:n.541-2161_541-2159deli...
ENST00000526417.6:n.528-2161_528-2159delinsCTT
ENST00000527070.5:c.*1156-2161_*1156-2159delinsCTT ENSP00000435149.1:n.*1156-2161_*1156-2159...
ENST00000532206.1:n.645-4864_645-4862delinsCTT
NM_001293557.1:c.460-2161_460-2159delinsCTT NP_001280486.1:n.460-2161_460-2159delinsC...
NM_022162.2:c.541-2161_541-2159delinsCTT NP_071445.1:n.541-2161_541-2159delinsCTT
XM_005256084.2:c.460-2161_460-2159delinsCTT XP_005256141.1:n.460-2161_460-2159delinsC...
XM_006721242.2:c.460-2161_460-2159delinsCTT XP_006721305.1:n.460-2161_460-2159delinsC...
XM_006721243.2:c.460-2161_460-2159delinsCTT XP_006721306.1:n.460-2161_460-2159delinsC...
XM_011523257.1:c.-37-2161_-37-2159delinsCTT XP_011521559.1:n.-37-2161_-37-2159delinsC...
XM_011523258.1:c.-37-2161_-37-2159delinsCTT XP_011521560.1:n.-37-2161_-37-2159delinsC...
XM_011523259.1:c.-20-4864_-20-4862delinsCTT XP_011521561.1:n.-20-4864_-20-4862delinsC...
XM_011523260.1:c.460-2161_460-2159delinsCTT XP_011521562.1:n.460-2161_460-2159delinsC...
XM_011523261.1:c.460-2161_460-2159delinsCTT XP_011521563.1:n.460-2161_460-2159delinsC...
XR_429725.2:n.550-2161_550-2159delinsCTT
XR_429726.2:n.550-2161_550-2159delinsCTT
XR_933387.1:n.550-2161_550-2159delinsCTT
XM_005256084.4:c.460-2161_460-2159delinsCTT XP_005256141.1:n.460-2161_460-2159delinsC...
XM_006721242.4:c.460-2161_460-2159delinsCTT XP_006721305.1:n.460-2161_460-2159delinsC...
XM_006721243.4:c.460-2161_460-2159delinsCTT XP_006721306.1:n.460-2161_460-2159delinsC...
XM_011523259.2:c.-20-4864_-20-4862delinsCTT XP_011521561.1:n.-20-4864_-20-4862delinsC...
XM_011523260.3:c.460-2161_460-2159delinsCTT XP_011521562.1:n.460-2161_460-2159delinsC...
XM_011523261.2:c.460-2161_460-2159delinsCTT XP_011521563.1:n.460-2161_460-2159delinsC...
XM_017023536.1:c.-126-2161_-126-2159delinsCTT XP_016879025.1:n.-126-2161_-126-2159delin...
XM_017023537.1:c.-20-4864_-20-4862delinsCTT XP_016879026.1:n.-20-4864_-20-4862delinsC...
XM_017023538.1:c.-126-2161_-126-2159delinsCTT XP_016879027.1:n.-126-2161_-126-2159delin...
XR_429725.3:n.503-2161_503-2159delinsCTT
XR_429726.3:n.503-2161_503-2159delinsCTT
XR_933387.2:n.503-2161_503-2159delinsCTT
NM_001293557.2:c.460-2161_460-2159delinsCTT NP_001280486.1:n.460-2161_460-2159delinsC...
NM_001370466.1:c.460-2161_460-2159delinsCTT MANE Select NP_001357395.1:n.460-2161_460-2159delinsC...
NM_022162.3:c.541-2161_541-2159delinsCTT NP_071445.1:n.541-2161_541-2159delinsCTT
NR_163434.1:n.525-2161_525-2159delinsCTT