Canonical Allele Identifier: CA395865738
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50699626A>C , CM000678.2:g.50699626A>C GRCh38
NC_000016.9:g.50733537A>C , CM000678.1:g.50733537A>C GRCh37
NC_000016.8:g.49291038A>C NCBI36
NG_007508.1:g.7488A>C , LRG_177:g.7488A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.131A>C ENSP00000493088.1:p.Tyr44Ser
ENST00000646677.2:c.131A>C ENSP00000496533.1:p.Tyr44Ser
ENST00000641284.1:c.131A>C ENSP00000493088.1:p.Tyr44Ser
ENST00000646677.1:c.131A>C ENSP00000496533.1:p.Tyr44Ser
ENST00000647318.2:c.131A>C MANE Select ENSP00000495993.1:p.Tyr44Ser
ENST00000300589.6:c.212A>C ENSP00000300589.2:p.Tyr71Ser
ENST00000526417.6:n.199A>C
ENST00000527070.5:c.*827A>C ENSP00000435149.1:n.*827A>C
ENST00000531674.1:c.131A>C ENSP00000431681.1:p.Tyr44Ser
ENST00000532206.1:n.316A>C
NM_001293557.1:c.131A>C NP_001280486.1:p.Tyr44Ser
NM_022162.2:c.212A>C NP_071445.1:p.Tyr71Ser
XM_005256084.2:c.131A>C XP_005256141.1:p.Tyr44Ser
XM_006721242.2:c.131A>C XP_006721305.1:p.Tyr44Ser
XM_006721243.2:c.131A>C XP_006721306.1:p.Tyr44Ser
XM_011523258.1:c.-38+5964A>C XP_011521560.1:n.-38+5964A>C
XM_011523259.1:c.-349A>C XP_011521561.1:n.-349A>C
XM_011523260.1:c.131A>C XP_011521562.1:p.Tyr44Ser
XM_011523261.1:c.131A>C XP_011521563.1:p.Tyr44Ser
XR_429725.2:n.221A>C
XR_429726.2:n.221A>C
XR_933387.1:n.221A>C
XM_005256084.4:c.131A>C XP_005256141.1:p.Tyr44Ser
XM_006721242.4:c.131A>C XP_006721305.1:p.Tyr44Ser
XM_006721243.4:c.131A>C XP_006721306.1:p.Tyr44Ser
XM_011523259.2:c.-349A>C XP_011521561.1:n.-349A>C
XM_011523260.3:c.131A>C XP_011521562.1:p.Tyr44Ser
XM_011523261.2:c.131A>C XP_011521563.1:p.Tyr44Ser
XM_017023536.1:c.-127+5964A>C XP_016879025.1:n.-127+5964A>C
XM_017023537.1:c.-21+5964A>C XP_016879026.1:n.-21+5964A>C
XR_429725.3:n.174A>C
XR_429726.3:n.174A>C
XR_933387.2:n.174A>C
NM_001293557.2:c.131A>C NP_001280486.1:p.Tyr44Ser
NM_001370466.1:c.131A>C MANE Select NP_001357395.1:p.Tyr44Ser
NM_022162.3:c.212A>C NP_071445.1:p.Tyr71Ser
NR_163434.1:n.196A>C