Canonical Allele Identifier: CA2221861516

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50711497_50711499delinsACT , CM000678.2:g.50711497_50711499delinsACT	GRCh38
NC_000016.9:g.50745408_50745410delinsACT , CM000678.1:g.50745408_50745410delinsACT	GRCh37
NC_000016.8:g.49302909_49302911delinsACT	NCBI36
NG_007508.1:g.19359_19361delinsACT , LRG_177:g.19359_19361delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.1505_1507delinsACT	ENSP00000493088.1:p.Asp502=
ENST00000646677.2:c.1505_1507delinsACT	ENSP00000496533.1:p.Asp502=
ENST00000641284.1:c.1505_1507delinsACT	ENSP00000493088.1:p.Asp502=
ENST00000646677.1:c.1505_1507delinsACT	ENSP00000496533.1:p.Asp502=
ENST00000647318.2:c.1505_1507delinsACT MANE Select	ENSP00000495993.1:p.Asp502=
ENST00000300589.6:c.1586_1588delinsACT	ENSP00000300589.2:p.Asp529=
NM_001293557.1:c.1505_1507delinsACT	NP_001280486.1:p.Asp502=
NM_022162.2:c.1586_1588delinsACT	NP_071445.1:p.Asp529=
XM_005256084.2:c.1505_1507delinsACT	XP_005256141.1:p.Asp502=
XM_006721242.2:c.1505_1507delinsACT	XP_006721305.1:p.Asp502=
XM_006721243.2:c.1505_1507delinsACT	XP_006721306.1:p.Asp502=
XM_011523257.1:c.1082_1084delinsACT	XP_011521559.1:p.Asp361=
XM_011523258.1:c.1082_1084delinsACT	XP_011521560.1:p.Asp361=
XM_011523259.1:c.920_922delinsACT	XP_011521561.1:p.Asp307=
XM_011523260.1:c.1505_1507delinsACT	XP_011521562.1:p.Asp502=
XM_011523261.1:c.1505_1507delinsACT	XP_011521563.1:p.Asp502=
XR_429725.2:n.1595_1597delinsACT
XR_429726.2:n.1595_1597delinsACT
XR_933387.1:n.1595_1597delinsACT
XM_005256084.4:c.1505_1507delinsACT	XP_005256141.1:p.Asp502=
XM_006721242.4:c.1505_1507delinsACT	XP_006721305.1:p.Asp502=
XM_006721243.4:c.1505_1507delinsACT	XP_006721306.1:p.Asp502=
XM_011523259.2:c.920_922delinsACT	XP_011521561.1:p.Asp307=
XM_011523260.3:c.1505_1507delinsACT	XP_011521562.1:p.Asp502=
XM_011523261.2:c.1505_1507delinsACT	XP_011521563.1:p.Asp502=
XM_017023535.1:c.1013_1015delinsACT	XP_016879024.1:p.Asp338=
XM_017023536.1:c.920_922delinsACT	XP_016879025.1:p.Asp307=
XM_017023537.1:c.920_922delinsACT	XP_016879026.1:p.Asp307=
XM_017023538.1:c.920_922delinsACT	XP_016879027.1:p.Asp307=
XR_429725.3:n.1548_1550delinsACT
XR_429726.3:n.1548_1550delinsACT
XR_933387.2:n.1548_1550delinsACT
NM_001293557.2:c.1505_1507delinsACT	NP_001280486.1:p.Asp502=
NM_001370466.1:c.1505_1507delinsACT MANE Select	NP_001357395.1:p.Asp502=
NM_022162.3:c.1586_1588delinsACT	NP_071445.1:p.Asp529=
NR_163434.1:n.1570_1572delinsACT