Canonical Allele Identifier: CA2221841637

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722690G= , CM000678.2:g.50722690G=	GRCh38
NC_000016.9:g.50756601G= , CM000678.1:g.50756601G=	GRCh37
NC_000016.8:g.49314102G=	NCBI36
NG_007508.1:g.30552G= , LRG_177:g.30552G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7128G=	ENSP00000493088.1:n.2382-7128G=
ENST00000646677.2:c.*467G=	ENSP00000496533.1:n.*467G=
ENST00000697425.1:c.529G=
ENST00000697426.1:c.417G=
ENST00000697427.1:c.333G=
ENST00000697428.1:n.2180G=
ENST00000641284.1:c.2382-7128G=	ENSP00000493088.1:n.2382-7128G=
ENST00000646677.1:c.*467G=	ENSP00000496533.1:n.*467G=
ENST00000647318.2:c.2702G= MANE Select	ENSP00000495993.1:p.Ser901=
ENST00000300589.6:c.2783G=	ENSP00000300589.2:p.Ser928=
ENST00000524712.5:c.277G=
ENST00000527052.5:c.249G=
ENST00000529633.5:c.361G=
ENST00000534057.1:c.417G=
ENST00000534067.5:c.513G=
NM_001293557.1:c.2702G=	NP_001280486.1:p.Ser901=
NM_022162.2:c.2783G=	NP_071445.1:p.Ser928=
XM_005256084.2:c.2702G=	XP_005256141.1:p.Ser901=
XM_006721242.2:c.2618G=	XP_006721305.1:p.Ser873=
XM_011523257.1:c.2279G=	XP_011521559.1:p.Ser760=
XM_011523258.1:c.2279G=	XP_011521560.1:p.Ser760=
XM_011523259.1:c.2117G=	XP_011521561.1:p.Ser706=
XR_429725.2:n.2624G=
XR_429726.2:n.2540G=
XR_933387.1:n.2820G=
XM_005256084.4:c.2702G=	XP_005256141.1:p.Ser901=
XM_006721242.4:c.2618G=	XP_006721305.1:p.Ser873=
XM_011523259.2:c.2117G=	XP_011521561.1:p.Ser706=
XM_017023535.1:c.2210G=	XP_016879024.1:p.Ser737=
XM_017023536.1:c.2117G=	XP_016879025.1:p.Ser706=
XM_017023537.1:c.2117G=	XP_016879026.1:p.Ser706=
XM_017023538.1:c.2117G=	XP_016879027.1:p.Ser706=
XR_429725.3:n.2577G=
XR_429726.3:n.2493G=
XR_933387.2:n.2773G=
NM_001293557.2:c.2702G=	NP_001280486.1:p.Ser901=
NM_001370466.1:c.2702G= MANE Select	NP_001357395.1:p.Ser901=
NM_022162.3:c.2783G=	NP_071445.1:p.Ser928=
NR_163434.1:n.2914G=