Canonical Allele Identifier: CA2221859132

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50710646G= , CM000678.2:g.50710646G=	GRCh38
NC_000016.9:g.50744557G= , CM000678.1:g.50744557G=	GRCh37
NC_000016.8:g.49302058G=	NCBI36
NG_007508.1:g.18508G= , LRG_177:g.18508G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.654G=	ENSP00000493088.1:p.Thr218=
ENST00000646677.2:c.654G=	ENSP00000496533.1:p.Thr218=
ENST00000641284.1:c.654G=	ENSP00000493088.1:p.Thr218=
ENST00000646677.1:c.654G=	ENSP00000496533.1:p.Thr218=
ENST00000647318.2:c.654G= MANE Select	ENSP00000495993.1:p.Thr218=
ENST00000300589.6:c.735G=	ENSP00000300589.2:p.Thr245=
ENST00000526417.6:n.795G=
ENST00000527070.5:c.*1350G=	ENSP00000435149.1:n.*1350G=
ENST00000532206.1:n.733G=
NM_001293557.1:c.654G=	NP_001280486.1:p.Thr218=
NM_022162.2:c.735G=	NP_071445.1:p.Thr245=
XM_005256084.2:c.654G=	XP_005256141.1:p.Thr218=
XM_006721242.2:c.654G=	XP_006721305.1:p.Thr218=
XM_006721243.2:c.654G=	XP_006721306.1:p.Thr218=
XM_011523257.1:c.231G=	XP_011521559.1:p.Thr77=
XM_011523258.1:c.231G=	XP_011521560.1:p.Thr77=
XM_011523259.1:c.69G=	XP_011521561.1:p.Thr23=
XM_011523260.1:c.654G=	XP_011521562.1:p.Thr218=
XM_011523261.1:c.654G=	XP_011521563.1:p.Thr218=
XR_429725.2:n.744G=
XR_429726.2:n.744G=
XR_933387.1:n.744G=
XM_005256084.4:c.654G=	XP_005256141.1:p.Thr218=
XM_006721242.4:c.654G=	XP_006721305.1:p.Thr218=
XM_006721243.4:c.654G=	XP_006721306.1:p.Thr218=
XM_011523259.2:c.69G=	XP_011521561.1:p.Thr23=
XM_011523260.3:c.654G=	XP_011521562.1:p.Thr218=
XM_011523261.2:c.654G=	XP_011521563.1:p.Thr218=
XM_017023535.1:c.162G=	XP_016879024.1:p.Thr54=
XM_017023536.1:c.69G=	XP_016879025.1:p.Thr23=
XM_017023537.1:c.69G=	XP_016879026.1:p.Thr23=
XM_017023538.1:c.69G=	XP_016879027.1:p.Thr23=
XR_429725.3:n.697G=
XR_429726.3:n.697G=
XR_933387.2:n.697G=
NM_001293557.2:c.654G=	NP_001280486.1:p.Thr218=
NM_001370466.1:c.654G= MANE Select	NP_001357395.1:p.Thr218=
NM_022162.3:c.735G=	NP_071445.1:p.Thr245=
NR_163434.1:n.719G=