Canonical Allele Identifier: CA2221841541
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722678G= , CM000678.2:g.50722678G= GRCh38
NC_000016.9:g.50756589G= , CM000678.1:g.50756589G= GRCh37
NC_000016.8:g.49314090G= NCBI36
NG_007508.1:g.30540G= , LRG_177:g.30540G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7140G= ENSP00000493088.1:n.2382-7140G=
ENST00000646677.2:c.*455G= ENSP00000496533.1:n.*455G=
ENST00000697425.1:c.517G=
ENST00000697426.1:c.405G=
ENST00000697427.1:c.321G=
ENST00000697428.1:n.2168G=
ENST00000641284.1:c.2382-7140G= ENSP00000493088.1:n.2382-7140G=
ENST00000646677.1:c.*455G= ENSP00000496533.1:n.*455G=
ENST00000647318.2:c.2690G= MANE Select ENSP00000495993.1:p.Gly897=
ENST00000300589.6:c.2771G= ENSP00000300589.2:p.Gly924=
ENST00000524712.5:c.265G=
ENST00000527052.5:c.237G=
ENST00000529633.5:c.349G=
ENST00000534057.1:c.405G=
ENST00000534067.5:c.501G=
NM_001293557.1:c.2690G= NP_001280486.1:p.Gly897=
NM_022162.2:c.2771G= NP_071445.1:p.Gly924=
XM_005256084.2:c.2690G= XP_005256141.1:p.Gly897=
XM_006721242.2:c.2606G= XP_006721305.1:p.Gly869=
XM_011523257.1:c.2267G= XP_011521559.1:p.Gly756=
XM_011523258.1:c.2267G= XP_011521560.1:p.Gly756=
XM_011523259.1:c.2105G= XP_011521561.1:p.Gly702=
XR_429725.2:n.2612G=
XR_429726.2:n.2528G=
XR_933387.1:n.2808G=
XM_005256084.4:c.2690G= XP_005256141.1:p.Gly897=
XM_006721242.4:c.2606G= XP_006721305.1:p.Gly869=
XM_011523259.2:c.2105G= XP_011521561.1:p.Gly702=
XM_017023535.1:c.2198G= XP_016879024.1:p.Gly733=
XM_017023536.1:c.2105G= XP_016879025.1:p.Gly702=
XM_017023537.1:c.2105G= XP_016879026.1:p.Gly702=
XM_017023538.1:c.2105G= XP_016879027.1:p.Gly702=
XR_429725.3:n.2565G=
XR_429726.3:n.2481G=
XR_933387.2:n.2761G=
NM_001293557.2:c.2690G= NP_001280486.1:p.Gly897=
NM_001370466.1:c.2690G= MANE Select NP_001357395.1:p.Gly897=
NM_022162.3:c.2771G= NP_071445.1:p.Gly924=
NR_163434.1:n.2902G=