Canonical Allele Identifier: CA395875038
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722634C>A , CM000678.2:g.50722634C>A GRCh38
NC_000016.9:g.50756545C>A , CM000678.1:g.50756545C>A GRCh37
NC_000016.8:g.49314046C>A NCBI36
NG_007508.1:g.30496C>A , LRG_177:g.30496C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7184C>A ENSP00000493088.1:n.2382-7184C>A
ENST00000646677.2:c.*411C>A ENSP00000496533.1:n.*411C>A
ENST00000697425.1:c.473C>A
ENST00000697426.1:c.361C>A
ENST00000697427.1:c.277C>A
ENST00000697428.1:n.2124C>A
ENST00000641284.1:c.2382-7184C>A ENSP00000493088.1:n.2382-7184C>A
ENST00000646677.1:c.*411C>A ENSP00000496533.1:n.*411C>A
ENST00000647318.2:c.2646C>A MANE Select ENSP00000495993.1:p.Asn882Lys
ENST00000300589.6:c.2727C>A ENSP00000300589.2:p.Asn909Lys
ENST00000524712.5:c.221C>A
ENST00000527052.5:c.193C>A
ENST00000529633.5:c.305C>A
ENST00000534057.1:c.361C>A
ENST00000534067.5:c.457C>A
NM_001293557.1:c.2646C>A NP_001280486.1:p.Asn882Lys
NM_022162.2:c.2727C>A NP_071445.1:p.Asn909Lys
XM_005256084.2:c.2646C>A XP_005256141.1:p.Asn882Lys
XM_006721242.2:c.2562C>A XP_006721305.1:p.Asn854Lys
XM_011523257.1:c.2223C>A XP_011521559.1:p.Asn741Lys
XM_011523258.1:c.2223C>A XP_011521560.1:p.Asn741Lys
XM_011523259.1:c.2061C>A XP_011521561.1:p.Asn687Lys
XR_429725.2:n.2568C>A
XR_429726.2:n.2484C>A
XR_933387.1:n.2764C>A
XM_005256084.4:c.2646C>A XP_005256141.1:p.Asn882Lys
XM_006721242.4:c.2562C>A XP_006721305.1:p.Asn854Lys
XM_011523259.2:c.2061C>A XP_011521561.1:p.Asn687Lys
XM_017023535.1:c.2154C>A XP_016879024.1:p.Asn718Lys
XM_017023536.1:c.2061C>A XP_016879025.1:p.Asn687Lys
XM_017023537.1:c.2061C>A XP_016879026.1:p.Asn687Lys
XM_017023538.1:c.2061C>A XP_016879027.1:p.Asn687Lys
XR_429725.3:n.2521C>A
XR_429726.3:n.2437C>A
XR_933387.2:n.2717C>A
NM_001293557.2:c.2646C>A NP_001280486.1:p.Asn882Lys
NM_001370466.1:c.2646C>A MANE Select NP_001357395.1:p.Asn882Lys
NM_022162.3:c.2727C>A NP_071445.1:p.Asn909Lys
NR_163434.1:n.2858C>A