Canonical Allele Identifier: CA721331355

Gene: NOD2

Linked Data

• dbSNP Id: rs1353234532
• MyVariant Identifiers: chr16:g.50737856_50737858del (hg19) ; chr16:g.50703945_50703947del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50703948_50703950del , CM000678.2:g.50703948_50703950del	GRCh38
NC_000016.9:g.50737859_50737861del , CM000678.1:g.50737859_50737861del	GRCh37
NC_000016.8:g.49295360_49295362del	NCBI36
NG_007508.1:g.11810_11812del , LRG_177:g.11810_11812del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.460-3907_460-3905del	ENSP00000493088.1:n.460-3907_460-3905del
ENST00000646677.2:c.460-3907_460-3905del	ENSP00000496533.1:n.460-3907_460-3905del
ENST00000641284.1:c.460-3907_460-3905del	ENSP00000493088.1:n.460-3907_460-3905del
ENST00000646677.1:c.460-3907_460-3905del	ENSP00000496533.1:n.460-3907_460-3905del
ENST00000647318.2:c.460-3907_460-3905del MANE Select	ENSP00000495993.1:n.460-3907_460-3905del
ENST00000300589.6:c.541-3907_541-3905del	ENSP00000300589.2:n.541-3907_541-3905del
ENST00000526417.6:n.528-3907_528-3905del
ENST00000527070.5:c.*1156-3907_*1156-3905del	ENSP00000435149.1:n.*1156-3907_*1156-3905del
ENST00000532206.1:n.644+3994_644+3996del
NM_001293557.1:c.460-3907_460-3905del	NP_001280486.1:n.460-3907_460-3905del
NM_022162.2:c.541-3907_541-3905del	NP_071445.1:n.541-3907_541-3905del
XM_005256084.2:c.460-3907_460-3905del	XP_005256141.1:n.460-3907_460-3905del
XM_006721242.2:c.460-3907_460-3905del	XP_006721305.1:n.460-3907_460-3905del
XM_006721243.2:c.460-3907_460-3905del	XP_006721306.1:n.460-3907_460-3905del
XM_011523257.1:c.-37-3907_-37-3905del	XP_011521559.1:n.-37-3907_-37-3905del
XM_011523258.1:c.-37-3907_-37-3905del	XP_011521560.1:n.-37-3907_-37-3905del
XM_011523259.1:c.-21+3994_-21+3996del	XP_011521561.1:n.-21+3994_-21+3996del
XM_011523260.1:c.460-3907_460-3905del	XP_011521562.1:n.460-3907_460-3905del
XM_011523261.1:c.460-3907_460-3905del	XP_011521563.1:n.460-3907_460-3905del
XR_429725.2:n.550-3907_550-3905del
XR_429726.2:n.550-3907_550-3905del
XR_933387.1:n.550-3907_550-3905del
XM_005256084.4:c.460-3907_460-3905del	XP_005256141.1:n.460-3907_460-3905del
XM_006721242.4:c.460-3907_460-3905del	XP_006721305.1:n.460-3907_460-3905del
XM_006721243.4:c.460-3907_460-3905del	XP_006721306.1:n.460-3907_460-3905del
XM_011523259.2:c.-21+3994_-21+3996del	XP_011521561.1:n.-21+3994_-21+3996del
XM_011523260.3:c.460-3907_460-3905del	XP_011521562.1:n.460-3907_460-3905del
XM_011523261.2:c.460-3907_460-3905del	XP_011521563.1:n.460-3907_460-3905del
XM_017023536.1:c.-126-3907_-126-3905del	XP_016879025.1:n.-126-3907_-126-3905del
XM_017023537.1:c.-20-6610_-20-6608del	XP_016879026.1:n.-20-6610_-20-6608del
XM_017023538.1:c.-127+3871_-127+3873del	XP_016879027.1:n.-127+3871_-127+3873del
XR_429725.3:n.503-3907_503-3905del
XR_429726.3:n.503-3907_503-3905del
XR_933387.2:n.503-3907_503-3905del
NM_001293557.2:c.460-3907_460-3905del	NP_001280486.1:n.460-3907_460-3905del
NM_001370466.1:c.460-3907_460-3905del MANE Select	NP_001357395.1:n.460-3907_460-3905del
NM_022162.3:c.541-3907_541-3905del	NP_071445.1:n.541-3907_541-3905del
NR_163434.1:n.525-3907_525-3905del