Canonical Allele Identifier: CA395869022
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50711396C>G , CM000678.2:g.50711396C>G GRCh38
NC_000016.9:g.50745307C>G , CM000678.1:g.50745307C>G GRCh37
NC_000016.8:g.49302808C>G NCBI36
NG_007508.1:g.19258C>G , LRG_177:g.19258C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.1404C>G ENSP00000493088.1:p.Cys468Trp
ENST00000646677.2:c.1404C>G ENSP00000496533.1:p.Cys468Trp
ENST00000641284.1:c.1404C>G ENSP00000493088.1:p.Cys468Trp
ENST00000646677.1:c.1404C>G ENSP00000496533.1:p.Cys468Trp
ENST00000647318.2:c.1404C>G MANE Select ENSP00000495993.1:p.Cys468Trp
ENST00000300589.6:c.1485C>G ENSP00000300589.2:p.Cys495Trp
NM_001293557.1:c.1404C>G NP_001280486.1:p.Cys468Trp
NM_022162.2:c.1485C>G NP_071445.1:p.Cys495Trp
XM_005256084.2:c.1404C>G XP_005256141.1:p.Cys468Trp
XM_006721242.2:c.1404C>G XP_006721305.1:p.Cys468Trp
XM_006721243.2:c.1404C>G XP_006721306.1:p.Cys468Trp
XM_011523257.1:c.981C>G XP_011521559.1:p.Cys327Trp
XM_011523258.1:c.981C>G XP_011521560.1:p.Cys327Trp
XM_011523259.1:c.819C>G XP_011521561.1:p.Cys273Trp
XM_011523260.1:c.1404C>G XP_011521562.1:p.Cys468Trp
XM_011523261.1:c.1404C>G XP_011521563.1:p.Cys468Trp
XR_429725.2:n.1494C>G
XR_429726.2:n.1494C>G
XR_933387.1:n.1494C>G
XM_005256084.4:c.1404C>G XP_005256141.1:p.Cys468Trp
XM_006721242.4:c.1404C>G XP_006721305.1:p.Cys468Trp
XM_006721243.4:c.1404C>G XP_006721306.1:p.Cys468Trp
XM_011523259.2:c.819C>G XP_011521561.1:p.Cys273Trp
XM_011523260.3:c.1404C>G XP_011521562.1:p.Cys468Trp
XM_011523261.2:c.1404C>G XP_011521563.1:p.Cys468Trp
XM_017023535.1:c.912C>G XP_016879024.1:p.Cys304Trp
XM_017023536.1:c.819C>G XP_016879025.1:p.Cys273Trp
XM_017023537.1:c.819C>G XP_016879026.1:p.Cys273Trp
XM_017023538.1:c.819C>G XP_016879027.1:p.Cys273Trp
XR_429725.3:n.1447C>G
XR_429726.3:n.1447C>G
XR_933387.2:n.1447C>G
NM_001293557.2:c.1404C>G NP_001280486.1:p.Cys468Trp
NM_001370466.1:c.1404C>G MANE Select NP_001357395.1:p.Cys468Trp
NM_022162.3:c.1485C>G NP_071445.1:p.Cys495Trp
NR_163434.1:n.1469C>G