Canonical Allele Identifier: CA2221841654

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722697G= , CM000678.2:g.50722697G=	GRCh38
NC_000016.9:g.50756608G= , CM000678.1:g.50756608G=	GRCh37
NC_000016.8:g.49314109G=	NCBI36
NG_007508.1:g.30559G= , LRG_177:g.30559G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7121G=	ENSP00000493088.1:n.2382-7121G=
ENST00000646677.2:c.*474G=	ENSP00000496533.1:n.*474G=
ENST00000697425.1:c.536G=
ENST00000697426.1:c.424G=
ENST00000697427.1:c.340G=
ENST00000697428.1:n.2187G=
ENST00000641284.1:c.2382-7121G=	ENSP00000493088.1:n.2382-7121G=
ENST00000646677.1:c.*474G=	ENSP00000496533.1:n.*474G=
ENST00000647318.2:c.2709G= MANE Select	ENSP00000495993.1:p.Arg903=
ENST00000300589.6:c.2790G=	ENSP00000300589.2:p.Arg930=
ENST00000524712.5:c.284G=
ENST00000527052.5:c.256G=
ENST00000529633.5:c.368G=
ENST00000534057.1:c.424G=
ENST00000534067.5:c.520G=
NM_001293557.1:c.2709G=	NP_001280486.1:p.Arg903=
NM_022162.2:c.2790G=	NP_071445.1:p.Arg930=
XM_005256084.2:c.2709G=	XP_005256141.1:p.Arg903=
XM_006721242.2:c.2625G=	XP_006721305.1:p.Arg875=
XM_011523257.1:c.2286G=	XP_011521559.1:p.Arg762=
XM_011523258.1:c.2286G=	XP_011521560.1:p.Arg762=
XM_011523259.1:c.2124G=	XP_011521561.1:p.Arg708=
XR_429725.2:n.2631G=
XR_429726.2:n.2547G=
XR_933387.1:n.2827G=
XM_005256084.4:c.2709G=	XP_005256141.1:p.Arg903=
XM_006721242.4:c.2625G=	XP_006721305.1:p.Arg875=
XM_011523259.2:c.2124G=	XP_011521561.1:p.Arg708=
XM_017023535.1:c.2217G=	XP_016879024.1:p.Arg739=
XM_017023536.1:c.2124G=	XP_016879025.1:p.Arg708=
XM_017023537.1:c.2124G=	XP_016879026.1:p.Arg708=
XM_017023538.1:c.2124G=	XP_016879027.1:p.Arg708=
XR_429725.3:n.2584G=
XR_429726.3:n.2500G=
XR_933387.2:n.2780G=
NM_001293557.2:c.2709G=	NP_001280486.1:p.Arg903=
NM_001370466.1:c.2709G= MANE Select	NP_001357395.1:p.Arg903=
NM_022162.3:c.2790G=	NP_071445.1:p.Arg930=
NR_163434.1:n.2921G=