Canonical Allele Identifier: CA2221867186

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50729818G= , CM000678.2:g.50729818G=	GRCh38
NC_000016.9:g.50763729G= , CM000678.1:g.50763729G=	GRCh37
NC_000016.8:g.49321230G=	NCBI36
NG_007508.1:g.37680G= , LRG_177:g.37680G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.2382G=	ENSP00000493088.1:p.Ter794=
ENST00000646677.2:c.*651G=	ENSP00000496533.1:n.*651G=
ENST00000697428.1:n.2364G=
ENST00000641284.1:c.2382G=	ENSP00000493088.1:p.Ter794=
ENST00000646677.1:c.*651G=	ENSP00000496533.1:n.*651G=
ENST00000647318.2:c.2886G= MANE Select	ENSP00000495993.1:p.Lys962=
ENST00000300589.6:c.2967G=	ENSP00000300589.2:p.Lys989=
NM_001293557.1:c.2886G=	NP_001280486.1:p.Lys962=
NM_022162.2:c.2967G=	NP_071445.1:p.Lys989=
XM_005256084.2:c.2886G=	XP_005256141.1:p.Lys962=
XM_006721242.2:c.2802G=	XP_006721305.1:p.Lys934=
XM_011523257.1:c.2463G=	XP_011521559.1:p.Lys821=
XM_011523258.1:c.2463G=	XP_011521560.1:p.Lys821=
XM_011523259.1:c.2301G=	XP_011521561.1:p.Lys767=
XM_005256084.4:c.2886G=	XP_005256141.1:p.Lys962=
XM_006721242.4:c.2802G=	XP_006721305.1:p.Lys934=
XM_011523259.2:c.2301G=	XP_011521561.1:p.Lys767=
XM_017023535.1:c.2394G=	XP_016879024.1:p.Lys798=
XM_017023536.1:c.2301G=	XP_016879025.1:p.Lys767=
XM_017023537.1:c.2301G=	XP_016879026.1:p.Lys767=
XM_017023538.1:c.2301G=	XP_016879027.1:p.Lys767=
NM_001293557.2:c.2886G=	NP_001280486.1:p.Lys962=
NM_001370466.1:c.2886G= MANE Select	NP_001357395.1:p.Lys962=
NM_022162.3:c.2967G=	NP_071445.1:p.Lys989=
NR_163434.1:n.3098G=