Canonical Allele Identifier: CA395868976
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50711376T>C , CM000678.2:g.50711376T>C GRCh38
NC_000016.9:g.50745287T>C , CM000678.1:g.50745287T>C GRCh37
NC_000016.8:g.49302788T>C NCBI36
NG_007508.1:g.19238T>C , LRG_177:g.19238T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.1384T>C ENSP00000493088.1:p.Ser462Pro
ENST00000646677.2:c.1384T>C ENSP00000496533.1:p.Ser462Pro
ENST00000641284.1:c.1384T>C ENSP00000493088.1:p.Ser462Pro
ENST00000646677.1:c.1384T>C ENSP00000496533.1:p.Ser462Pro
ENST00000647318.2:c.1384T>C MANE Select ENSP00000495993.1:p.Ser462Pro
ENST00000300589.6:c.1465T>C ENSP00000300589.2:p.Ser489Pro
NM_001293557.1:c.1384T>C NP_001280486.1:p.Ser462Pro
NM_022162.2:c.1465T>C NP_071445.1:p.Ser489Pro
XM_005256084.2:c.1384T>C XP_005256141.1:p.Ser462Pro
XM_006721242.2:c.1384T>C XP_006721305.1:p.Ser462Pro
XM_006721243.2:c.1384T>C XP_006721306.1:p.Ser462Pro
XM_011523257.1:c.961T>C XP_011521559.1:p.Ser321Pro
XM_011523258.1:c.961T>C XP_011521560.1:p.Ser321Pro
XM_011523259.1:c.799T>C XP_011521561.1:p.Ser267Pro
XM_011523260.1:c.1384T>C XP_011521562.1:p.Ser462Pro
XM_011523261.1:c.1384T>C XP_011521563.1:p.Ser462Pro
XR_429725.2:n.1474T>C
XR_429726.2:n.1474T>C
XR_933387.1:n.1474T>C
XM_005256084.4:c.1384T>C XP_005256141.1:p.Ser462Pro
XM_006721242.4:c.1384T>C XP_006721305.1:p.Ser462Pro
XM_006721243.4:c.1384T>C XP_006721306.1:p.Ser462Pro
XM_011523259.2:c.799T>C XP_011521561.1:p.Ser267Pro
XM_011523260.3:c.1384T>C XP_011521562.1:p.Ser462Pro
XM_011523261.2:c.1384T>C XP_011521563.1:p.Ser462Pro
XM_017023535.1:c.892T>C XP_016879024.1:p.Ser298Pro
XM_017023536.1:c.799T>C XP_016879025.1:p.Ser267Pro
XM_017023537.1:c.799T>C XP_016879026.1:p.Ser267Pro
XM_017023538.1:c.799T>C XP_016879027.1:p.Ser267Pro
XR_429725.3:n.1427T>C
XR_429726.3:n.1427T>C
XR_933387.2:n.1427T>C
NM_001293557.2:c.1384T>C NP_001280486.1:p.Ser462Pro
NM_001370466.1:c.1384T>C MANE Select NP_001357395.1:p.Ser462Pro
NM_022162.3:c.1465T>C NP_071445.1:p.Ser489Pro
NR_163434.1:n.1449T>C