Canonical Allele Identifier: CA2221849908

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50705676_50705686delinsGCTGATCATTC , CM000678.2:g.50705676_50705686delinsGCTGATCATTC	GRCh38
NC_000016.9:g.50739587_50739597delinsGCTGATCATTC , CM000678.1:g.50739587_50739597delinsGCTGATCATTC	GRCh37
NC_000016.8:g.49297088_49297098delinsGCTGATCATTC	NCBI36
NG_007508.1:g.13538_13548delinsGCTGATCATTC , LRG_177:g.13538_13548delinsGCTGATCATTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.460-2179_460-2169delinsGCTGATCATTC	ENSP00000493088.1:n.460-2179_460-2169deli...
ENST00000646677.2:c.460-2179_460-2169delinsGCTGATCATTC	ENSP00000496533.1:n.460-2179_460-2169deli...
ENST00000641284.1:c.460-2179_460-2169delinsGCTGATCATTC	ENSP00000493088.1:n.460-2179_460-2169deli...
ENST00000646677.1:c.460-2179_460-2169delinsGCTGATCATTC	ENSP00000496533.1:n.460-2179_460-2169deli...
ENST00000647318.2:c.460-2179_460-2169delinsGCTGATCATTC MANE Select	ENSP00000495993.1:n.460-2179_460-2169deli...
ENST00000300589.6:c.541-2179_541-2169delinsGCTGATCATTC	ENSP00000300589.2:n.541-2179_541-2169deli...
ENST00000526417.6:n.528-2179_528-2169delinsGCTGATCATTC
ENST00000527070.5:c.*1156-2179_*1156-2169delinsGCTGATCATTC	ENSP00000435149.1:n.*1156-2179_*1156-2169...
ENST00000532206.1:n.645-4882_645-4872delinsGCTGATCATTC
NM_001293557.1:c.460-2179_460-2169delinsGCTGATCATTC	NP_001280486.1:n.460-2179_460-2169delinsG...
NM_022162.2:c.541-2179_541-2169delinsGCTGATCATTC	NP_071445.1:n.541-2179_541-2169delinsGCTG...
XM_005256084.2:c.460-2179_460-2169delinsGCTGATCATTC	XP_005256141.1:n.460-2179_460-2169delinsG...
XM_006721242.2:c.460-2179_460-2169delinsGCTGATCATTC	XP_006721305.1:n.460-2179_460-2169delinsG...
XM_006721243.2:c.460-2179_460-2169delinsGCTGATCATTC	XP_006721306.1:n.460-2179_460-2169delinsG...
XM_011523257.1:c.-37-2179_-37-2169delinsGCTGATCATTC	XP_011521559.1:n.-37-2179_-37-2169delinsG...
XM_011523258.1:c.-37-2179_-37-2169delinsGCTGATCATTC	XP_011521560.1:n.-37-2179_-37-2169delinsG...
XM_011523259.1:c.-20-4882_-20-4872delinsGCTGATCATTC	XP_011521561.1:n.-20-4882_-20-4872delinsG...
XM_011523260.1:c.460-2179_460-2169delinsGCTGATCATTC	XP_011521562.1:n.460-2179_460-2169delinsG...
XM_011523261.1:c.460-2179_460-2169delinsGCTGATCATTC	XP_011521563.1:n.460-2179_460-2169delinsG...
XR_429725.2:n.550-2179_550-2169delinsGCTGATCATTC
XR_429726.2:n.550-2179_550-2169delinsGCTGATCATTC
XR_933387.1:n.550-2179_550-2169delinsGCTGATCATTC
XM_005256084.4:c.460-2179_460-2169delinsGCTGATCATTC	XP_005256141.1:n.460-2179_460-2169delinsG...
XM_006721242.4:c.460-2179_460-2169delinsGCTGATCATTC	XP_006721305.1:n.460-2179_460-2169delinsG...
XM_006721243.4:c.460-2179_460-2169delinsGCTGATCATTC	XP_006721306.1:n.460-2179_460-2169delinsG...
XM_011523259.2:c.-20-4882_-20-4872delinsGCTGATCATTC	XP_011521561.1:n.-20-4882_-20-4872delinsG...
XM_011523260.3:c.460-2179_460-2169delinsGCTGATCATTC	XP_011521562.1:n.460-2179_460-2169delinsG...
XM_011523261.2:c.460-2179_460-2169delinsGCTGATCATTC	XP_011521563.1:n.460-2179_460-2169delinsG...
XM_017023536.1:c.-126-2179_-126-2169delinsGCTGATCATTC	XP_016879025.1:n.-126-2179_-126-2169delin...
XM_017023537.1:c.-20-4882_-20-4872delinsGCTGATCATTC	XP_016879026.1:n.-20-4882_-20-4872delinsG...
XM_017023538.1:c.-126-2179_-126-2169delinsGCTGATCATTC	XP_016879027.1:n.-126-2179_-126-2169delin...
XR_429725.3:n.503-2179_503-2169delinsGCTGATCATTC
XR_429726.3:n.503-2179_503-2169delinsGCTGATCATTC
XR_933387.2:n.503-2179_503-2169delinsGCTGATCATTC
NM_001293557.2:c.460-2179_460-2169delinsGCTGATCATTC	NP_001280486.1:n.460-2179_460-2169delinsG...
NM_001370466.1:c.460-2179_460-2169delinsGCTGATCATTC MANE Select	NP_001357395.1:n.460-2179_460-2169delinsG...
NM_022162.3:c.541-2179_541-2169delinsGCTGATCATTC	NP_071445.1:n.541-2179_541-2169delinsGCTG...
NR_163434.1:n.525-2179_525-2169delinsGCTGATCATTC