Canonical Allele Identifier: CA2221859035

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50710614C= , CM000678.2:g.50710614C=	GRCh38
NC_000016.9:g.50744525C= , CM000678.1:g.50744525C=	GRCh37
NC_000016.8:g.49302026C=	NCBI36
NG_007508.1:g.18476C= , LRG_177:g.18476C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.622C=	ENSP00000493088.1:p.Arg208=
ENST00000646677.2:c.622C=	ENSP00000496533.1:p.Arg208=
ENST00000641284.1:c.622C=	ENSP00000493088.1:p.Arg208=
ENST00000646677.1:c.622C=	ENSP00000496533.1:p.Arg208=
ENST00000647318.2:c.622C= MANE Select	ENSP00000495993.1:p.Arg208=
ENST00000300589.6:c.703C=	ENSP00000300589.2:p.Arg235=
ENST00000526417.6:n.763C=
ENST00000527070.5:c.*1318C=	ENSP00000435149.1:n.*1318C=
ENST00000532206.1:n.701C=
NM_001293557.1:c.622C=	NP_001280486.1:p.Arg208=
NM_022162.2:c.703C=	NP_071445.1:p.Arg235=
XM_005256084.2:c.622C=	XP_005256141.1:p.Arg208=
XM_006721242.2:c.622C=	XP_006721305.1:p.Arg208=
XM_006721243.2:c.622C=	XP_006721306.1:p.Arg208=
XM_011523257.1:c.199C=	XP_011521559.1:p.Arg67=
XM_011523258.1:c.199C=	XP_011521560.1:p.Arg67=
XM_011523259.1:c.37C=	XP_011521561.1:p.Arg13=
XM_011523260.1:c.622C=	XP_011521562.1:p.Arg208=
XM_011523261.1:c.622C=	XP_011521563.1:p.Arg208=
XR_429725.2:n.712C=
XR_429726.2:n.712C=
XR_933387.1:n.712C=
XM_005256084.4:c.622C=	XP_005256141.1:p.Arg208=
XM_006721242.4:c.622C=	XP_006721305.1:p.Arg208=
XM_006721243.4:c.622C=	XP_006721306.1:p.Arg208=
XM_011523259.2:c.37C=	XP_011521561.1:p.Arg13=
XM_011523260.3:c.622C=	XP_011521562.1:p.Arg208=
XM_011523261.2:c.622C=	XP_011521563.1:p.Arg208=
XM_017023535.1:c.130C=	XP_016879024.1:p.Arg44=
XM_017023536.1:c.37C=	XP_016879025.1:p.Arg13=
XM_017023537.1:c.37C=	XP_016879026.1:p.Arg13=
XM_017023538.1:c.37C=	XP_016879027.1:p.Arg13=
XR_429725.3:n.665C=
XR_429726.3:n.665C=
XR_933387.2:n.665C=
NM_001293557.2:c.622C=	NP_001280486.1:p.Arg208=
NM_001370466.1:c.622C= MANE Select	NP_001357395.1:p.Arg208=
NM_022162.3:c.703C=	NP_071445.1:p.Arg235=
NR_163434.1:n.687C=