Canonical Allele Identifier: CA2221859897
Community Standard Title: NM_001370466.1(NOD2):c.917G= (p.Cys306=)
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50710909G= , CM000678.2:g.50710909G= GRCh38
NC_000016.9:g.50744820G= , CM000678.1:g.50744820G= GRCh37
NC_000016.8:g.49302321G= NCBI36
NG_007508.1:g.18771G= , LRG_177:g.18771G=

Transcript Alleles

HGVS Amino-acid Change
NM_001370466.1:c.917G= MANE Select NP_001357395.1:p.Cys306=
ENST00000647318.2:c.917G= MANE Select ENSP00000495993.1:p.Cys306=
NM_001293557.1:c.917G= NP_001280486.1:p.Cys306=
NM_001293557.2:c.917G= NP_001280486.1:p.Cys306=
NM_022162.2:c.998G= NP_071445.1:p.Cys333=
NM_022162.3:c.998G= NP_071445.1:p.Cys333=
NR_163434.1:n.982G=
ENST00000300589.6:c.998G= ENSP00000300589.2:p.Cys333=
ENST00000526417.6:n.1058G=
ENST00000641284.1:c.917G= ENSP00000493088.1:p.Cys306=
ENST00000641284.2:c.917G= ENSP00000493088.1:p.Cys306=
ENST00000646677.1:c.917G= ENSP00000496533.1:p.Cys306=
ENST00000646677.2:c.917G= ENSP00000496533.1:p.Cys306=
XM_005256084.2:c.917G= XP_005256141.1:p.Cys306=
XM_005256084.4:c.917G= XP_005256141.1:p.Cys306=
XM_006721242.2:c.917G= XP_006721305.1:p.Cys306=
XM_006721242.4:c.917G= XP_006721305.1:p.Cys306=
XM_006721243.2:c.917G= XP_006721306.1:p.Cys306=
XM_006721243.4:c.917G= XP_006721306.1:p.Cys306=
XM_011523257.1:c.494G= XP_011521559.1:p.Cys165=
XM_011523258.1:c.494G= XP_011521560.1:p.Cys165=
XM_011523259.1:c.332G= XP_011521561.1:p.Cys111=
XM_011523259.2:c.332G= XP_011521561.1:p.Cys111=
XM_011523260.1:c.917G= XP_011521562.1:p.Cys306=
XM_011523260.3:c.917G= XP_011521562.1:p.Cys306=
XM_011523261.1:c.917G= XP_011521563.1:p.Cys306=
XM_011523261.2:c.917G= XP_011521563.1:p.Cys306=
XM_017023535.1:c.425G= XP_016879024.1:p.Cys142=
XM_017023536.1:c.332G= XP_016879025.1:p.Cys111=
XM_017023537.1:c.332G= XP_016879026.1:p.Cys111=
XM_017023538.1:c.332G= XP_016879027.1:p.Cys111=
XR_429725.2:n.1007G=
XR_429725.3:n.960G=
XR_429726.2:n.1007G=
XR_429726.3:n.960G=
XR_933387.1:n.1007G=
XR_933387.2:n.960G=