Canonical Allele Identifier: CA2221858910
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50710528C= , CM000678.2:g.50710528C= GRCh38
NC_000016.9:g.50744439C= , CM000678.1:g.50744439C= GRCh37
NC_000016.8:g.49301940C= NCBI36
NG_007508.1:g.18390C= , LRG_177:g.18390C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.566-30C= ENSP00000493088.1:n.566-30C=
ENST00000646677.2:c.566-30C= ENSP00000496533.1:n.566-30C=
ENST00000641284.1:c.566-30C= ENSP00000493088.1:n.566-30C=
ENST00000646677.1:c.566-30C= ENSP00000496533.1:n.566-30C=
ENST00000647318.2:c.566-30C= MANE Select ENSP00000495993.1:n.566-30C=
ENST00000300589.6:c.647-30C= ENSP00000300589.2:n.647-30C=
ENST00000526417.6:n.707-30C=
ENST00000527070.5:c.*1262-30C= ENSP00000435149.1:n.*1262-30C=
ENST00000532206.1:n.645-30C=
NM_001293557.1:c.566-30C= NP_001280486.1:n.566-30C=
NM_022162.2:c.647-30C= NP_071445.1:n.647-30C=
XM_005256084.2:c.566-30C= XP_005256141.1:n.566-30C=
XM_006721242.2:c.566-30C= XP_006721305.1:n.566-30C=
XM_006721243.2:c.566-30C= XP_006721306.1:n.566-30C=
XM_011523257.1:c.143-30C= XP_011521559.1:n.143-30C=
XM_011523258.1:c.143-30C= XP_011521560.1:n.143-30C=
XM_011523259.1:c.-20-30C= XP_011521561.1:n.-20-30C=
XM_011523260.1:c.566-30C= XP_011521562.1:n.566-30C=
XM_011523261.1:c.566-30C= XP_011521563.1:n.566-30C=
XR_429725.2:n.656-30C=
XR_429726.2:n.656-30C=
XR_933387.1:n.656-30C=
XM_005256084.4:c.566-30C= XP_005256141.1:n.566-30C=
XM_006721242.4:c.566-30C= XP_006721305.1:n.566-30C=
XM_006721243.4:c.566-30C= XP_006721306.1:n.566-30C=
XM_011523259.2:c.-20-30C= XP_011521561.1:n.-20-30C=
XM_011523260.3:c.566-30C= XP_011521562.1:n.566-30C=
XM_011523261.2:c.566-30C= XP_011521563.1:n.566-30C=
XM_017023535.1:c.74-30C= XP_016879024.1:n.74-30C=
XM_017023536.1:c.-20-30C= XP_016879025.1:n.-20-30C=
XM_017023537.1:c.-20-30C= XP_016879026.1:n.-20-30C=
XM_017023538.1:c.-20-30C= XP_016879027.1:n.-20-30C=
XR_429725.3:n.609-30C=
XR_429726.3:n.609-30C=
XR_933387.2:n.609-30C=
NM_001293557.2:c.566-30C= NP_001280486.1:n.566-30C=
NM_001370466.1:c.566-30C= MANE Select NP_001357395.1:n.566-30C=
NM_022162.3:c.647-30C= NP_071445.1:n.647-30C=
NR_163434.1:n.631-30C=