Canonical Allele Identifier: CA2221841317

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722629G= , CM000678.2:g.50722629G=	GRCh38
NC_000016.9:g.50756540G= , CM000678.1:g.50756540G=	GRCh37
NC_000016.8:g.49314041G=	NCBI36
NG_007508.1:g.30491G= , LRG_177:g.30491G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001370466.1:c.2641G= MANE Select	NP_001357395.1:p.Gly881=
ENST00000647318.2:c.2641G= MANE Select	ENSP00000495993.1:p.Gly881=
NM_001293557.1:c.2641G=	NP_001280486.1:p.Gly881=
NM_001293557.2:c.2641G=	NP_001280486.1:p.Gly881=
NM_022162.2:c.2722G=	NP_071445.1:p.Gly908=
NM_022162.3:c.2722G=	NP_071445.1:p.Gly908=
NR_163434.1:n.2853G=
ENST00000300589.6:c.2722G=	ENSP00000300589.2:p.Gly908=
ENST00000524712.5:c.216G=
ENST00000527052.5:c.188G=
ENST00000529633.5:c.300G=
ENST00000534057.1:c.356G=
ENST00000534067.5:c.452G=
ENST00000641284.1:c.2382-7189G=	ENSP00000493088.1:n.2382-7189G=
ENST00000641284.2:c.2382-7189G=	ENSP00000493088.1:n.2382-7189G=
ENST00000646677.1:c.*406G=	ENSP00000496533.1:n.*406G=
ENST00000646677.2:c.*406G=	ENSP00000496533.1:n.*406G=
ENST00000697425.1:c.468G=
ENST00000697426.1:c.356G=
ENST00000697427.1:c.272G=
ENST00000697428.1:n.2119G=
XM_005256084.2:c.2641G=	XP_005256141.1:p.Gly881=
XM_005256084.4:c.2641G=	XP_005256141.1:p.Gly881=
XM_006721242.2:c.2557G=	XP_006721305.1:p.Gly853=
XM_006721242.4:c.2557G=	XP_006721305.1:p.Gly853=
XM_011523257.1:c.2218G=	XP_011521559.1:p.Gly740=
XM_011523258.1:c.2218G=	XP_011521560.1:p.Gly740=
XM_011523259.1:c.2056G=	XP_011521561.1:p.Gly686=
XM_011523259.2:c.2056G=	XP_011521561.1:p.Gly686=
XM_017023535.1:c.2149G=	XP_016879024.1:p.Gly717=
XM_017023536.1:c.2056G=	XP_016879025.1:p.Gly686=
XM_017023537.1:c.2056G=	XP_016879026.1:p.Gly686=
XM_017023538.1:c.2056G=	XP_016879027.1:p.Gly686=
XR_429725.2:n.2563G=
XR_429725.3:n.2516G=
XR_429726.2:n.2479G=
XR_429726.3:n.2432G=
XR_933387.1:n.2759G=
XR_933387.2:n.2712G=