Canonical Allele Identifier: CA2221841254
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722624T= , CM000678.2:g.50722624T= GRCh38
NC_000016.9:g.50756535T= , CM000678.1:g.50756535T= GRCh37
NC_000016.8:g.49314036T= NCBI36
NG_007508.1:g.30486T= , LRG_177:g.30486T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7194T= ENSP00000493088.1:n.2382-7194T=
ENST00000646677.2:c.*401T= ENSP00000496533.1:n.*401T=
ENST00000697425.1:c.463T=
ENST00000697426.1:c.351T=
ENST00000697427.1:c.267T=
ENST00000697428.1:n.2114T=
ENST00000641284.1:c.2382-7194T= ENSP00000493088.1:n.2382-7194T=
ENST00000646677.1:c.*401T= ENSP00000496533.1:n.*401T=
ENST00000647318.2:c.2636T= MANE Select ENSP00000495993.1:p.Phe879=
ENST00000300589.6:c.2717T= ENSP00000300589.2:p.Phe906=
ENST00000524712.5:c.211T=
ENST00000527052.5:c.183T=
ENST00000529633.5:c.295T=
ENST00000534057.1:c.351T=
ENST00000534067.5:c.447T=
NM_001293557.1:c.2636T= NP_001280486.1:p.Phe879=
NM_022162.2:c.2717T= NP_071445.1:p.Phe906=
XM_005256084.2:c.2636T= XP_005256141.1:p.Phe879=
XM_006721242.2:c.2552T= XP_006721305.1:p.Phe851=
XM_011523257.1:c.2213T= XP_011521559.1:p.Phe738=
XM_011523258.1:c.2213T= XP_011521560.1:p.Phe738=
XM_011523259.1:c.2051T= XP_011521561.1:p.Phe684=
XR_429725.2:n.2558T=
XR_429726.2:n.2474T=
XR_933387.1:n.2754T=
XM_005256084.4:c.2636T= XP_005256141.1:p.Phe879=
XM_006721242.4:c.2552T= XP_006721305.1:p.Phe851=
XM_011523259.2:c.2051T= XP_011521561.1:p.Phe684=
XM_017023535.1:c.2144T= XP_016879024.1:p.Phe715=
XM_017023536.1:c.2051T= XP_016879025.1:p.Phe684=
XM_017023537.1:c.2051T= XP_016879026.1:p.Phe684=
XM_017023538.1:c.2051T= XP_016879027.1:p.Phe684=
XR_429725.3:n.2511T=
XR_429726.3:n.2427T=
XR_933387.2:n.2707T=
NM_001293557.2:c.2636T= NP_001280486.1:p.Phe879=
NM_001370466.1:c.2636T= MANE Select NP_001357395.1:p.Phe879=
NM_022162.3:c.2717T= NP_071445.1:p.Phe906=
NR_163434.1:n.2848T=