Canonical Allele Identifier: CA2221845433
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50704130_50704131delinsCT , CM000678.2:g.50704130_50704131delinsCT GRCh38
NC_000016.9:g.50738041_50738042delinsCT , CM000678.1:g.50738041_50738042delinsCT GRCh37
NC_000016.8:g.49295542_49295543delinsCT NCBI36
NG_007508.1:g.11992_11993delinsCT , LRG_177:g.11992_11993delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.460-3725_460-3724delinsCT ENSP00000493088.1:n.460-3725_460-3724deli...
ENST00000646677.2:c.460-3725_460-3724delinsCT ENSP00000496533.1:n.460-3725_460-3724deli...
ENST00000641284.1:c.460-3725_460-3724delinsCT ENSP00000493088.1:n.460-3725_460-3724deli...
ENST00000646677.1:c.460-3725_460-3724delinsCT ENSP00000496533.1:n.460-3725_460-3724deli...
ENST00000647318.2:c.460-3725_460-3724delinsCT MANE Select ENSP00000495993.1:n.460-3725_460-3724deli...
ENST00000300589.6:c.541-3725_541-3724delinsCT ENSP00000300589.2:n.541-3725_541-3724deli...
ENST00000526417.6:n.528-3725_528-3724delinsCT
ENST00000527070.5:c.*1156-3725_*1156-3724delinsCT ENSP00000435149.1:n.*1156-3725_*1156-3724...
ENST00000532206.1:n.644+4176_644+4177delinsCT
NM_001293557.1:c.460-3725_460-3724delinsCT NP_001280486.1:n.460-3725_460-3724delinsC...
NM_022162.2:c.541-3725_541-3724delinsCT NP_071445.1:n.541-3725_541-3724delinsCT
XM_005256084.2:c.460-3725_460-3724delinsCT XP_005256141.1:n.460-3725_460-3724delinsC...
XM_006721242.2:c.460-3725_460-3724delinsCT XP_006721305.1:n.460-3725_460-3724delinsC...
XM_006721243.2:c.460-3725_460-3724delinsCT XP_006721306.1:n.460-3725_460-3724delinsC...
XM_011523257.1:c.-37-3725_-37-3724delinsCT XP_011521559.1:n.-37-3725_-37-3724delinsC...
XM_011523258.1:c.-37-3725_-37-3724delinsCT XP_011521560.1:n.-37-3725_-37-3724delinsC...
XM_011523259.1:c.-21+4176_-21+4177delinsCT XP_011521561.1:n.-21+4176_-21+4177delinsC...
XM_011523260.1:c.460-3725_460-3724delinsCT XP_011521562.1:n.460-3725_460-3724delinsC...
XM_011523261.1:c.460-3725_460-3724delinsCT XP_011521563.1:n.460-3725_460-3724delinsC...
XR_429725.2:n.550-3725_550-3724delinsCT
XR_429726.2:n.550-3725_550-3724delinsCT
XR_933387.1:n.550-3725_550-3724delinsCT
XM_005256084.4:c.460-3725_460-3724delinsCT XP_005256141.1:n.460-3725_460-3724delinsC...
XM_006721242.4:c.460-3725_460-3724delinsCT XP_006721305.1:n.460-3725_460-3724delinsC...
XM_006721243.4:c.460-3725_460-3724delinsCT XP_006721306.1:n.460-3725_460-3724delinsC...
XM_011523259.2:c.-21+4176_-21+4177delinsCT XP_011521561.1:n.-21+4176_-21+4177delinsC...
XM_011523260.3:c.460-3725_460-3724delinsCT XP_011521562.1:n.460-3725_460-3724delinsC...
XM_011523261.2:c.460-3725_460-3724delinsCT XP_011521563.1:n.460-3725_460-3724delinsC...
XM_017023536.1:c.-126-3725_-126-3724delinsCT XP_016879025.1:n.-126-3725_-126-3724delin...
XM_017023537.1:c.-20-6428_-20-6427delinsCT XP_016879026.1:n.-20-6428_-20-6427delinsC...
XM_017023538.1:c.-126-3725_-126-3724delinsCT XP_016879027.1:n.-126-3725_-126-3724delin...
XR_429725.3:n.503-3725_503-3724delinsCT
XR_429726.3:n.503-3725_503-3724delinsCT
XR_933387.2:n.503-3725_503-3724delinsCT
NM_001293557.2:c.460-3725_460-3724delinsCT NP_001280486.1:n.460-3725_460-3724delinsC...
NM_001370466.1:c.460-3725_460-3724delinsCT MANE Select NP_001357395.1:n.460-3725_460-3724delinsC...
NM_022162.3:c.541-3725_541-3724delinsCT NP_071445.1:n.541-3725_541-3724delinsCT
NR_163434.1:n.525-3725_525-3724delinsCT