Canonical Allele Identifier: CA2221862242

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50711880A= , CM000678.2:g.50711880A=	GRCh38
NC_000016.9:g.50745791A= , CM000678.1:g.50745791A=	GRCh37
NC_000016.8:g.49303292A=	NCBI36
NG_007508.1:g.19742A= , LRG_177:g.19742A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.1888A=	ENSP00000493088.1:p.Ser630=
ENST00000646677.2:c.1888A=	ENSP00000496533.1:p.Ser630=
ENST00000641284.1:c.1888A=	ENSP00000493088.1:p.Ser630=
ENST00000646677.1:c.1888A=	ENSP00000496533.1:p.Ser630=
ENST00000647318.2:c.1888A= MANE Select	ENSP00000495993.1:p.Ser630=
ENST00000300589.6:c.1969A=	ENSP00000300589.2:p.Ser657=
NM_001293557.1:c.1888A=	NP_001280486.1:p.Ser630=
NM_022162.2:c.1969A=	NP_071445.1:p.Ser657=
XM_005256084.2:c.1888A=	XP_005256141.1:p.Ser630=
XM_006721242.2:c.1888A=	XP_006721305.1:p.Ser630=
XM_006721243.2:c.1888A=	XP_006721306.1:p.Ser630=
XM_011523257.1:c.1465A=	XP_011521559.1:p.Ser489=
XM_011523258.1:c.1465A=	XP_011521560.1:p.Ser489=
XM_011523259.1:c.1303A=	XP_011521561.1:p.Ser435=
XM_011523260.1:c.1888A=	XP_011521562.1:p.Ser630=
XM_011523261.1:c.1888A=	XP_011521563.1:p.Ser630=
XR_429725.2:n.1978A=
XR_429726.2:n.1978A=
XR_933387.1:n.1978A=
XM_005256084.4:c.1888A=	XP_005256141.1:p.Ser630=
XM_006721242.4:c.1888A=	XP_006721305.1:p.Ser630=
XM_006721243.4:c.1888A=	XP_006721306.1:p.Ser630=
XM_011523259.2:c.1303A=	XP_011521561.1:p.Ser435=
XM_011523260.3:c.1888A=	XP_011521562.1:p.Ser630=
XM_011523261.2:c.1888A=	XP_011521563.1:p.Ser630=
XM_017023535.1:c.1396A=	XP_016879024.1:p.Ser466=
XM_017023536.1:c.1303A=	XP_016879025.1:p.Ser435=
XM_017023537.1:c.1303A=	XP_016879026.1:p.Ser435=
XM_017023538.1:c.1303A=	XP_016879027.1:p.Ser435=
XR_429725.3:n.1931A=
XR_429726.3:n.1931A=
XR_933387.2:n.1931A=
NM_001293557.2:c.1888A=	NP_001280486.1:p.Ser630=
NM_001370466.1:c.1888A= MANE Select	NP_001357395.1:p.Ser630=
NM_022162.3:c.1969A=	NP_071445.1:p.Ser657=
NR_163434.1:n.1953A=