Canonical Allele Identifier: CA395875034
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722633A>G , CM000678.2:g.50722633A>G GRCh38
NC_000016.9:g.50756544A>G , CM000678.1:g.50756544A>G GRCh37
NC_000016.8:g.49314045A>G NCBI36
NG_007508.1:g.30495A>G , LRG_177:g.30495A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7185A>G ENSP00000493088.1:n.2382-7185A>G
ENST00000646677.2:c.*410A>G ENSP00000496533.1:n.*410A>G
ENST00000697425.1:c.472A>G
ENST00000697426.1:c.360A>G
ENST00000697427.1:c.276A>G
ENST00000697428.1:n.2123A>G
ENST00000641284.1:c.2382-7185A>G ENSP00000493088.1:n.2382-7185A>G
ENST00000646677.1:c.*410A>G ENSP00000496533.1:n.*410A>G
ENST00000647318.2:c.2645A>G MANE Select ENSP00000495993.1:p.Asn882Ser
ENST00000300589.6:c.2726A>G ENSP00000300589.2:p.Asn909Ser
ENST00000524712.5:c.220A>G
ENST00000527052.5:c.192A>G
ENST00000529633.5:c.304A>G
ENST00000534057.1:c.360A>G
ENST00000534067.5:c.456A>G
NM_001293557.1:c.2645A>G NP_001280486.1:p.Asn882Ser
NM_022162.2:c.2726A>G NP_071445.1:p.Asn909Ser
XM_005256084.2:c.2645A>G XP_005256141.1:p.Asn882Ser
XM_006721242.2:c.2561A>G XP_006721305.1:p.Asn854Ser
XM_011523257.1:c.2222A>G XP_011521559.1:p.Asn741Ser
XM_011523258.1:c.2222A>G XP_011521560.1:p.Asn741Ser
XM_011523259.1:c.2060A>G XP_011521561.1:p.Asn687Ser
XR_429725.2:n.2567A>G
XR_429726.2:n.2483A>G
XR_933387.1:n.2763A>G
XM_005256084.4:c.2645A>G XP_005256141.1:p.Asn882Ser
XM_006721242.4:c.2561A>G XP_006721305.1:p.Asn854Ser
XM_011523259.2:c.2060A>G XP_011521561.1:p.Asn687Ser
XM_017023535.1:c.2153A>G XP_016879024.1:p.Asn718Ser
XM_017023536.1:c.2060A>G XP_016879025.1:p.Asn687Ser
XM_017023537.1:c.2060A>G XP_016879026.1:p.Asn687Ser
XM_017023538.1:c.2060A>G XP_016879027.1:p.Asn687Ser
XR_429725.3:n.2520A>G
XR_429726.3:n.2436A>G
XR_933387.2:n.2716A>G
NM_001293557.2:c.2645A>G NP_001280486.1:p.Asn882Ser
NM_001370466.1:c.2645A>G MANE Select NP_001357395.1:p.Asn882Ser
NM_022162.3:c.2726A>G NP_071445.1:p.Asn909Ser
NR_163434.1:n.2857A>G