Canonical Allele Identifier: CA395875023
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722630G>A , CM000678.2:g.50722630G>A GRCh38
NC_000016.9:g.50756541G>A , CM000678.1:g.50756541G>A GRCh37
NC_000016.8:g.49314042G>A NCBI36
NG_007508.1:g.30492G>A , LRG_177:g.30492G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7188G>A ENSP00000493088.1:n.2382-7188G>A
ENST00000646677.2:c.*407G>A ENSP00000496533.1:n.*407G>A
ENST00000697425.1:c.469G>A
ENST00000697426.1:c.357G>A
ENST00000697427.1:c.273G>A
ENST00000697428.1:n.2120G>A
ENST00000641284.1:c.2382-7188G>A ENSP00000493088.1:n.2382-7188G>A
ENST00000646677.1:c.*407G>A ENSP00000496533.1:n.*407G>A
ENST00000647318.2:c.2642G>A MANE Select ENSP00000495993.1:p.Gly881Asp
ENST00000300589.6:c.2723G>A ENSP00000300589.2:p.Gly908Asp
ENST00000524712.5:c.217G>A
ENST00000527052.5:c.189G>A
ENST00000529633.5:c.301G>A
ENST00000534057.1:c.357G>A
ENST00000534067.5:c.453G>A
NM_001293557.1:c.2642G>A NP_001280486.1:p.Gly881Asp
NM_022162.2:c.2723G>A NP_071445.1:p.Gly908Asp
XM_005256084.2:c.2642G>A XP_005256141.1:p.Gly881Asp
XM_006721242.2:c.2558G>A XP_006721305.1:p.Gly853Asp
XM_011523257.1:c.2219G>A XP_011521559.1:p.Gly740Asp
XM_011523258.1:c.2219G>A XP_011521560.1:p.Gly740Asp
XM_011523259.1:c.2057G>A XP_011521561.1:p.Gly686Asp
XR_429725.2:n.2564G>A
XR_429726.2:n.2480G>A
XR_933387.1:n.2760G>A
XM_005256084.4:c.2642G>A XP_005256141.1:p.Gly881Asp
XM_006721242.4:c.2558G>A XP_006721305.1:p.Gly853Asp
XM_011523259.2:c.2057G>A XP_011521561.1:p.Gly686Asp
XM_017023535.1:c.2150G>A XP_016879024.1:p.Gly717Asp
XM_017023536.1:c.2057G>A XP_016879025.1:p.Gly686Asp
XM_017023537.1:c.2057G>A XP_016879026.1:p.Gly686Asp
XM_017023538.1:c.2057G>A XP_016879027.1:p.Gly686Asp
XR_429725.3:n.2517G>A
XR_429726.3:n.2433G>A
XR_933387.2:n.2713G>A
NM_001293557.2:c.2642G>A NP_001280486.1:p.Gly881Asp
NM_001370466.1:c.2642G>A MANE Select NP_001357395.1:p.Gly881Asp
NM_022162.3:c.2723G>A NP_071445.1:p.Gly908Asp
NR_163434.1:n.2854G>A