Canonical Allele Identifier: CA2837240864

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50711670_50711672delinsTGG , CM000678.2:g.50711670_50711672delinsTGG	GRCh38
NC_000016.9:g.50745581_50745583delinsTGG , CM000678.1:g.50745581_50745583delinsTGG	GRCh37
NC_000016.8:g.49303082_49303084delinsTGG	NCBI36
NG_007508.1:g.19532_19534delinsTGG , LRG_177:g.19532_19534delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.1678_1680delinsTGG	ENSP00000493088.1:p.Arg560Trp
ENST00000646677.2:c.1678_1680delinsTGG	ENSP00000496533.1:p.Arg560Trp
ENST00000641284.1:c.1678_1680delinsTGG	ENSP00000493088.1:p.Arg560Trp
ENST00000646677.1:c.1678_1680delinsTGG	ENSP00000496533.1:p.Arg560Trp
ENST00000647318.2:c.1678_1680delinsTGG MANE Select	ENSP00000495993.1:p.Arg560Trp
ENST00000300589.6:c.1759_1761delinsTGG	ENSP00000300589.2:p.Arg587Trp
NM_001293557.1:c.1678_1680delinsTGG	NP_001280486.1:p.Arg560Trp
NM_022162.2:c.1759_1761delinsTGG	NP_071445.1:p.Arg587Trp
XM_005256084.2:c.1678_1680delinsTGG	XP_005256141.1:p.Arg560Trp
XM_006721242.2:c.1678_1680delinsTGG	XP_006721305.1:p.Arg560Trp
XM_006721243.2:c.1678_1680delinsTGG	XP_006721306.1:p.Arg560Trp
XM_011523257.1:c.1255_1257delinsTGG	XP_011521559.1:p.Arg419Trp
XM_011523258.1:c.1255_1257delinsTGG	XP_011521560.1:p.Arg419Trp
XM_011523259.1:c.1093_1095delinsTGG	XP_011521561.1:p.Arg365Trp
XM_011523260.1:c.1678_1680delinsTGG	XP_011521562.1:p.Arg560Trp
XM_011523261.1:c.1678_1680delinsTGG	XP_011521563.1:p.Arg560Trp
XR_429725.2:n.1768_1770delinsTGG
XR_429726.2:n.1768_1770delinsTGG
XR_933387.1:n.1768_1770delinsTGG
XM_005256084.4:c.1678_1680delinsTGG	XP_005256141.1:p.Arg560Trp
XM_006721242.4:c.1678_1680delinsTGG	XP_006721305.1:p.Arg560Trp
XM_006721243.4:c.1678_1680delinsTGG	XP_006721306.1:p.Arg560Trp
XM_011523259.2:c.1093_1095delinsTGG	XP_011521561.1:p.Arg365Trp
XM_011523260.3:c.1678_1680delinsTGG	XP_011521562.1:p.Arg560Trp
XM_011523261.2:c.1678_1680delinsTGG	XP_011521563.1:p.Arg560Trp
XM_017023535.1:c.1186_1188delinsTGG	XP_016879024.1:p.Arg396Trp
XM_017023536.1:c.1093_1095delinsTGG	XP_016879025.1:p.Arg365Trp
XM_017023537.1:c.1093_1095delinsTGG	XP_016879026.1:p.Arg365Trp
XM_017023538.1:c.1093_1095delinsTGG	XP_016879027.1:p.Arg365Trp
XR_429725.3:n.1721_1723delinsTGG
XR_429726.3:n.1721_1723delinsTGG
XR_933387.2:n.1721_1723delinsTGG
NM_001293557.2:c.1678_1680delinsTGG	NP_001280486.1:p.Arg560Trp
NM_001370466.1:c.1678_1680delinsTGG MANE Select	NP_001357395.1:p.Arg560Trp
NM_022162.3:c.1759_1761delinsTGG	NP_071445.1:p.Arg587Trp
NR_163434.1:n.1743_1745delinsTGG