Canonical Allele Identifier: CA2221844923

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50703944_50703947delinsGGCT , CM000678.2:g.50703944_50703947delinsGGCT	GRCh38
NC_000016.9:g.50737855_50737858delinsGGCT , CM000678.1:g.50737855_50737858delinsGGCT	GRCh37
NC_000016.8:g.49295356_49295359delinsGGCT	NCBI36
NG_007508.1:g.11806_11809delinsGGCT , LRG_177:g.11806_11809delinsGGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.460-3911_460-3908delinsGGCT	ENSP00000493088.1:n.460-3911_460-3908delinsGGCT
ENST00000646677.2:c.460-3911_460-3908delinsGGCT	ENSP00000496533.1:n.460-3911_460-3908delinsGGCT
ENST00000641284.1:c.460-3911_460-3908delinsGGCT	ENSP00000493088.1:n.460-3911_460-3908delinsGGCT
ENST00000646677.1:c.460-3911_460-3908delinsGGCT	ENSP00000496533.1:n.460-3911_460-3908delinsGGCT
ENST00000647318.2:c.460-3911_460-3908delinsGGCT MANE Select	ENSP00000495993.1:n.460-3911_460-3908delinsGGCT
ENST00000300589.6:c.541-3911_541-3908delinsGGCT	ENSP00000300589.2:n.541-3911_541-3908delinsGGCT
ENST00000526417.6:n.528-3911_528-3908delinsGGCT
ENST00000527070.5:c.*1156-3911_*1156-3908delinsGGCT	ENSP00000435149.1:n.*1156-3911_*1156-3908delinsGGCT
ENST00000532206.1:n.644+3990_644+3993delinsGGCT
NM_001293557.1:c.460-3911_460-3908delinsGGCT	NP_001280486.1:n.460-3911_460-3908delinsGGCT
NM_022162.2:c.541-3911_541-3908delinsGGCT	NP_071445.1:n.541-3911_541-3908delinsGGCT
XM_005256084.2:c.460-3911_460-3908delinsGGCT	XP_005256141.1:n.460-3911_460-3908delinsGGCT
XM_006721242.2:c.460-3911_460-3908delinsGGCT	XP_006721305.1:n.460-3911_460-3908delinsGGCT
XM_006721243.2:c.460-3911_460-3908delinsGGCT	XP_006721306.1:n.460-3911_460-3908delinsGGCT
XM_011523257.1:c.-37-3911_-37-3908delinsGGCT	XP_011521559.1:n.-37-3911_-37-3908delinsGGCT
XM_011523258.1:c.-37-3911_-37-3908delinsGGCT	XP_011521560.1:n.-37-3911_-37-3908delinsGGCT
XM_011523259.1:c.-21+3990_-21+3993delinsGGCT	XP_011521561.1:n.-21+3990_-21+3993delinsGGCT
XM_011523260.1:c.460-3911_460-3908delinsGGCT	XP_011521562.1:n.460-3911_460-3908delinsGGCT
XM_011523261.1:c.460-3911_460-3908delinsGGCT	XP_011521563.1:n.460-3911_460-3908delinsGGCT
XR_429725.2:n.550-3911_550-3908delinsGGCT
XR_429726.2:n.550-3911_550-3908delinsGGCT
XR_933387.1:n.550-3911_550-3908delinsGGCT
XM_005256084.4:c.460-3911_460-3908delinsGGCT	XP_005256141.1:n.460-3911_460-3908delinsGGCT
XM_006721242.4:c.460-3911_460-3908delinsGGCT	XP_006721305.1:n.460-3911_460-3908delinsGGCT
XM_006721243.4:c.460-3911_460-3908delinsGGCT	XP_006721306.1:n.460-3911_460-3908delinsGGCT
XM_011523259.2:c.-21+3990_-21+3993delinsGGCT	XP_011521561.1:n.-21+3990_-21+3993delinsGGCT
XM_011523260.3:c.460-3911_460-3908delinsGGCT	XP_011521562.1:n.460-3911_460-3908delinsGGCT
XM_011523261.2:c.460-3911_460-3908delinsGGCT	XP_011521563.1:n.460-3911_460-3908delinsGGCT
XM_017023536.1:c.-126-3911_-126-3908delinsGGCT	XP_016879025.1:n.-126-3911_-126-3908delinsGGCT
XM_017023537.1:c.-20-6614_-20-6611delinsGGCT	XP_016879026.1:n.-20-6614_-20-6611delinsGGCT
XM_017023538.1:c.-127+3867_-127+3870delinsGGCT	XP_016879027.1:n.-127+3867_-127+3870delinsGGCT
XR_429725.3:n.503-3911_503-3908delinsGGCT
XR_429726.3:n.503-3911_503-3908delinsGGCT
XR_933387.2:n.503-3911_503-3908delinsGGCT
NM_001293557.2:c.460-3911_460-3908delinsGGCT	NP_001280486.1:n.460-3911_460-3908delinsGGCT
NM_001370466.1:c.460-3911_460-3908delinsGGCT MANE Select	NP_001357395.1:n.460-3911_460-3908delinsGGCT
NM_022162.3:c.541-3911_541-3908delinsGGCT	NP_071445.1:n.541-3911_541-3908delinsGGCT
NR_163434.1:n.525-3911_525-3908delinsGGCT