Canonical Allele Identifier: CA395875145
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722660C>G , CM000678.2:g.50722660C>G GRCh38
NC_000016.9:g.50756571C>G , CM000678.1:g.50756571C>G GRCh37
NC_000016.8:g.49314072C>G NCBI36
NG_007508.1:g.30522C>G , LRG_177:g.30522C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7158C>G ENSP00000493088.1:n.2382-7158C>G
ENST00000646677.2:c.*437C>G ENSP00000496533.1:n.*437C>G
ENST00000697425.1:c.499C>G
ENST00000697426.1:c.387C>G
ENST00000697427.1:c.303C>G
ENST00000697428.1:n.2150C>G
ENST00000641284.1:c.2382-7158C>G ENSP00000493088.1:n.2382-7158C>G
ENST00000646677.1:c.*437C>G ENSP00000496533.1:n.*437C>G
ENST00000647318.2:c.2672C>G MANE Select ENSP00000495993.1:p.Ala891Gly
ENST00000300589.6:c.2753C>G ENSP00000300589.2:p.Ala918Gly
ENST00000524712.5:c.247C>G
ENST00000527052.5:c.219C>G
ENST00000529633.5:c.331C>G
ENST00000534057.1:c.387C>G
ENST00000534067.5:c.483C>G
NM_001293557.1:c.2672C>G NP_001280486.1:p.Ala891Gly
NM_022162.2:c.2753C>G NP_071445.1:p.Ala918Gly
XM_005256084.2:c.2672C>G XP_005256141.1:p.Ala891Gly
XM_006721242.2:c.2588C>G XP_006721305.1:p.Ala863Gly
XM_011523257.1:c.2249C>G XP_011521559.1:p.Ala750Gly
XM_011523258.1:c.2249C>G XP_011521560.1:p.Ala750Gly
XM_011523259.1:c.2087C>G XP_011521561.1:p.Ala696Gly
XR_429725.2:n.2594C>G
XR_429726.2:n.2510C>G
XR_933387.1:n.2790C>G
XM_005256084.4:c.2672C>G XP_005256141.1:p.Ala891Gly
XM_006721242.4:c.2588C>G XP_006721305.1:p.Ala863Gly
XM_011523259.2:c.2087C>G XP_011521561.1:p.Ala696Gly
XM_017023535.1:c.2180C>G XP_016879024.1:p.Ala727Gly
XM_017023536.1:c.2087C>G XP_016879025.1:p.Ala696Gly
XM_017023537.1:c.2087C>G XP_016879026.1:p.Ala696Gly
XM_017023538.1:c.2087C>G XP_016879027.1:p.Ala696Gly
XR_429725.3:n.2547C>G
XR_429726.3:n.2463C>G
XR_933387.2:n.2743C>G
NM_001293557.2:c.2672C>G NP_001280486.1:p.Ala891Gly
NM_001370466.1:c.2672C>G MANE Select NP_001357395.1:p.Ala891Gly
NM_022162.3:c.2753C>G NP_071445.1:p.Ala918Gly
NR_163434.1:n.2884C>G