Canonical Allele Identifier: CA2221844403

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50703817_50703818delinsTC , CM000678.2:g.50703817_50703818delinsTC	GRCh38
NC_000016.9:g.50737728_50737729delinsTC , CM000678.1:g.50737728_50737729delinsTC	GRCh37
NC_000016.8:g.49295229_49295230delinsTC	NCBI36
NG_007508.1:g.11679_11680delinsTC , LRG_177:g.11679_11680delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.459+3863_459+3864delinsTC	ENSP00000493088.1:n.459+3863_459+3864delinsTC
ENST00000646677.2:c.459+3863_459+3864delinsTC	ENSP00000496533.1:n.459+3863_459+3864delinsTC
ENST00000641284.1:c.459+3863_459+3864delinsTC	ENSP00000493088.1:n.459+3863_459+3864delinsTC
ENST00000646677.1:c.459+3863_459+3864delinsTC	ENSP00000496533.1:n.459+3863_459+3864delinsTC
ENST00000647318.2:c.459+3863_459+3864delinsTC MANE Select	ENSP00000495993.1:n.459+3863_459+3864delinsTC
ENST00000300589.6:c.540+3863_540+3864delinsTC	ENSP00000300589.2:n.540+3863_540+3864delinsTC
ENST00000526417.6:n.527+3863_527+3864delinsTC
ENST00000527070.5:c.*1155+3863_*1155+3864delinsTC	ENSP00000435149.1:n.*1155+3863_*1155+3864delinsTC
ENST00000532206.1:n.644+3863_644+3864delinsTC
NM_001293557.1:c.459+3863_459+3864delinsTC	NP_001280486.1:n.459+3863_459+3864delinsTC
NM_022162.2:c.540+3863_540+3864delinsTC	NP_071445.1:n.540+3863_540+3864delinsTC
XM_005256084.2:c.459+3863_459+3864delinsTC	XP_005256141.1:n.459+3863_459+3864delinsTC
XM_006721242.2:c.459+3863_459+3864delinsTC	XP_006721305.1:n.459+3863_459+3864delinsTC
XM_006721243.2:c.459+3863_459+3864delinsTC	XP_006721306.1:n.459+3863_459+3864delinsTC
XM_011523257.1:c.-38+3863_-38+3864delinsTC	XP_011521559.1:n.-38+3863_-38+3864delinsTC
XM_011523258.1:c.-37-4038_-37-4037delinsTC	XP_011521560.1:n.-37-4038_-37-4037delinsTC
XM_011523259.1:c.-21+3863_-21+3864delinsTC	XP_011521561.1:n.-21+3863_-21+3864delinsTC
XM_011523260.1:c.459+3863_459+3864delinsTC	XP_011521562.1:n.459+3863_459+3864delinsTC
XM_011523261.1:c.459+3863_459+3864delinsTC	XP_011521563.1:n.459+3863_459+3864delinsTC
XR_429725.2:n.549+3863_549+3864delinsTC
XR_429726.2:n.549+3863_549+3864delinsTC
XR_933387.1:n.549+3863_549+3864delinsTC
XM_005256084.4:c.459+3863_459+3864delinsTC	XP_005256141.1:n.459+3863_459+3864delinsTC
XM_006721242.4:c.459+3863_459+3864delinsTC	XP_006721305.1:n.459+3863_459+3864delinsTC
XM_006721243.4:c.459+3863_459+3864delinsTC	XP_006721306.1:n.459+3863_459+3864delinsTC
XM_011523259.2:c.-21+3863_-21+3864delinsTC	XP_011521561.1:n.-21+3863_-21+3864delinsTC
XM_011523260.3:c.459+3863_459+3864delinsTC	XP_011521562.1:n.459+3863_459+3864delinsTC
XM_011523261.2:c.459+3863_459+3864delinsTC	XP_011521563.1:n.459+3863_459+3864delinsTC
XM_017023536.1:c.-126-4038_-126-4037delinsTC	XP_016879025.1:n.-126-4038_-126-4037delinsTC
XM_017023537.1:c.-20-6741_-20-6740delinsTC	XP_016879026.1:n.-20-6741_-20-6740delinsTC
XM_017023538.1:c.-127+3740_-127+3741delinsTC	XP_016879027.1:n.-127+3740_-127+3741delinsTC
XR_429725.3:n.502+3863_502+3864delinsTC
XR_429726.3:n.502+3863_502+3864delinsTC
XR_933387.2:n.502+3863_502+3864delinsTC
NM_001293557.2:c.459+3863_459+3864delinsTC	NP_001280486.1:n.459+3863_459+3864delinsTC
NM_001370466.1:c.459+3863_459+3864delinsTC MANE Select	NP_001357395.1:n.459+3863_459+3864delinsTC
NM_022162.3:c.540+3863_540+3864delinsTC	NP_071445.1:n.540+3863_540+3864delinsTC
NR_163434.1:n.524+3863_524+3864delinsTC