Canonical Allele Identifier: CA977234735
Gene: NOD2 HGNC NCBI

Linked Data

dbSNP Id: rs1963817051

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50699407del , CM000678.2:g.50699407del GRCh38
NC_000016.9:g.50733318del , CM000678.1:g.50733318del GRCh37
NC_000016.8:g.49290819del NCBI36
NG_007508.1:g.7269del , LRG_177:g.7269del

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.-8-81del ENSP00000493088.1:n.-8-81del
ENST00000646677.2:c.-8-81del ENSP00000496533.1:n.-8-81del
ENST00000641284.1:c.-8-81del ENSP00000493088.1:n.-8-81del
ENST00000646677.1:c.-8-81del ENSP00000496533.1:n.-8-81del
ENST00000647318.2:c.-8-81del MANE Select ENSP00000495993.1:n.-8-81del
ENST00000300589.6:c.74-81del ENSP00000300589.2:n.74-81del
ENST00000526417.6:n.61-81del
ENST00000527070.5:c.*689-81del ENSP00000435149.1:n.*689-81del
ENST00000531674.1:c.-8-81del ENSP00000431681.1:n.-8-81del
ENST00000532206.1:n.178-81del
NM_001293557.1:c.-89del NP_001280486.1:n.-89del
NM_022162.2:c.74-81del NP_071445.1:n.74-81del
XM_005256084.2:c.-8-81del XP_005256141.1:n.-8-81del
XM_006721242.2:c.-8-81del XP_006721305.1:n.-8-81del
XM_006721243.2:c.-8-81del XP_006721306.1:n.-8-81del
XM_011523258.1:c.-38+5745del XP_011521560.1:n.-38+5745del
XM_011523260.1:c.-8-81del XP_011521562.1:n.-8-81del
XM_011523261.1:c.-8-81del XP_011521563.1:n.-8-81del
XR_429725.2:n.83-81del
XR_429726.2:n.83-81del
XR_933387.1:n.83-81del
XM_005256084.4:c.-8-81del XP_005256141.1:n.-8-81del
XM_006721242.4:c.-8-81del XP_006721305.1:n.-8-81del
XM_006721243.4:c.-8-81del XP_006721306.1:n.-8-81del
XM_011523260.3:c.-8-81del XP_011521562.1:n.-8-81del
XM_011523261.2:c.-8-81del XP_011521563.1:n.-8-81del
XM_017023536.1:c.-127+5745del XP_016879025.1:n.-127+5745del
XM_017023537.1:c.-21+5745del XP_016879026.1:n.-21+5745del
XR_429725.3:n.36-81del
XR_429726.3:n.36-81del
XR_933387.2:n.36-81del
NM_001293557.2:c.-89del NP_001280486.1:n.-89del
NM_001370466.1:c.-8-81del MANE Select NP_001357395.1:n.-8-81del
NM_022162.3:c.74-81del NP_071445.1:n.74-81del
NR_163434.1:n.58-81del