Canonical Allele Identifier: CA395875082
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722645A>G , CM000678.2:g.50722645A>G GRCh38
NC_000016.9:g.50756556A>G , CM000678.1:g.50756556A>G GRCh37
NC_000016.8:g.49314057A>G NCBI36
NG_007508.1:g.30507A>G , LRG_177:g.30507A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7173A>G ENSP00000493088.1:n.2382-7173A>G
ENST00000646677.2:c.*422A>G ENSP00000496533.1:n.*422A>G
ENST00000697425.1:c.484A>G
ENST00000697426.1:c.372A>G
ENST00000697427.1:c.288A>G
ENST00000697428.1:n.2135A>G
ENST00000641284.1:c.2382-7173A>G ENSP00000493088.1:n.2382-7173A>G
ENST00000646677.1:c.*422A>G ENSP00000496533.1:n.*422A>G
ENST00000647318.2:c.2657A>G MANE Select ENSP00000495993.1:p.Asp886Gly
ENST00000300589.6:c.2738A>G ENSP00000300589.2:p.Asp913Gly
ENST00000524712.5:c.232A>G
ENST00000527052.5:c.204A>G
ENST00000529633.5:c.316A>G
ENST00000534057.1:c.372A>G
ENST00000534067.5:c.468A>G
NM_001293557.1:c.2657A>G NP_001280486.1:p.Asp886Gly
NM_022162.2:c.2738A>G NP_071445.1:p.Asp913Gly
XM_005256084.2:c.2657A>G XP_005256141.1:p.Asp886Gly
XM_006721242.2:c.2573A>G XP_006721305.1:p.Asp858Gly
XM_011523257.1:c.2234A>G XP_011521559.1:p.Asp745Gly
XM_011523258.1:c.2234A>G XP_011521560.1:p.Asp745Gly
XM_011523259.1:c.2072A>G XP_011521561.1:p.Asp691Gly
XR_429725.2:n.2579A>G
XR_429726.2:n.2495A>G
XR_933387.1:n.2775A>G
XM_005256084.4:c.2657A>G XP_005256141.1:p.Asp886Gly
XM_006721242.4:c.2573A>G XP_006721305.1:p.Asp858Gly
XM_011523259.2:c.2072A>G XP_011521561.1:p.Asp691Gly
XM_017023535.1:c.2165A>G XP_016879024.1:p.Asp722Gly
XM_017023536.1:c.2072A>G XP_016879025.1:p.Asp691Gly
XM_017023537.1:c.2072A>G XP_016879026.1:p.Asp691Gly
XM_017023538.1:c.2072A>G XP_016879027.1:p.Asp691Gly
XR_429725.3:n.2532A>G
XR_429726.3:n.2448A>G
XR_933387.2:n.2728A>G
NM_001293557.2:c.2657A>G NP_001280486.1:p.Asp886Gly
NM_001370466.1:c.2657A>G MANE Select NP_001357395.1:p.Asp886Gly
NM_022162.3:c.2738A>G NP_071445.1:p.Asp913Gly
NR_163434.1:n.2869A>G