Canonical Allele Identifier: CA2221841436

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722648A= , CM000678.2:g.50722648A=	GRCh38
NC_000016.9:g.50756559A= , CM000678.1:g.50756559A=	GRCh37
NC_000016.8:g.49314060A=	NCBI36
NG_007508.1:g.30510A= , LRG_177:g.30510A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7170A=	ENSP00000493088.1:n.2382-7170A=
ENST00000646677.2:c.*425A=	ENSP00000496533.1:n.*425A=
ENST00000697425.1:c.487A=
ENST00000697426.1:c.375A=
ENST00000697427.1:c.291A=
ENST00000697428.1:n.2138A=
ENST00000641284.1:c.2382-7170A=	ENSP00000493088.1:n.2382-7170A=
ENST00000646677.1:c.*425A=	ENSP00000496533.1:n.*425A=
ENST00000647318.2:c.2660A= MANE Select	ENSP00000495993.1:p.Glu887=
ENST00000300589.6:c.2741A=	ENSP00000300589.2:p.Glu914=
ENST00000524712.5:c.235A=
ENST00000527052.5:c.207A=
ENST00000529633.5:c.319A=
ENST00000534057.1:c.375A=
ENST00000534067.5:c.471A=
NM_001293557.1:c.2660A=	NP_001280486.1:p.Glu887=
NM_022162.2:c.2741A=	NP_071445.1:p.Glu914=
XM_005256084.2:c.2660A=	XP_005256141.1:p.Glu887=
XM_006721242.2:c.2576A=	XP_006721305.1:p.Glu859=
XM_011523257.1:c.2237A=	XP_011521559.1:p.Glu746=
XM_011523258.1:c.2237A=	XP_011521560.1:p.Glu746=
XM_011523259.1:c.2075A=	XP_011521561.1:p.Glu692=
XR_429725.2:n.2582A=
XR_429726.2:n.2498A=
XR_933387.1:n.2778A=
XM_005256084.4:c.2660A=	XP_005256141.1:p.Glu887=
XM_006721242.4:c.2576A=	XP_006721305.1:p.Glu859=
XM_011523259.2:c.2075A=	XP_011521561.1:p.Glu692=
XM_017023535.1:c.2168A=	XP_016879024.1:p.Glu723=
XM_017023536.1:c.2075A=	XP_016879025.1:p.Glu692=
XM_017023537.1:c.2075A=	XP_016879026.1:p.Glu692=
XM_017023538.1:c.2075A=	XP_016879027.1:p.Glu692=
XR_429725.3:n.2535A=
XR_429726.3:n.2451A=
XR_933387.2:n.2731A=
NM_001293557.2:c.2660A=	NP_001280486.1:p.Glu887=
NM_001370466.1:c.2660A= MANE Select	NP_001357395.1:p.Glu887=
NM_022162.3:c.2741A=	NP_071445.1:p.Glu914=
NR_163434.1:n.2872A=