Canonical Allele Identifier: CA2221834549

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50699660C= , CM000678.2:g.50699660C=	GRCh38
NC_000016.9:g.50733571C= , CM000678.1:g.50733571C=	GRCh37
NC_000016.8:g.49291072C=	NCBI36
NG_007508.1:g.7522C= , LRG_177:g.7522C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.165C=	ENSP00000493088.1:p.Ser55=
ENST00000646677.2:c.165C=	ENSP00000496533.1:p.Ser55=
ENST00000641284.1:c.165C=	ENSP00000493088.1:p.Ser55=
ENST00000646677.1:c.165C=	ENSP00000496533.1:p.Ser55=
ENST00000647318.2:c.165C= MANE Select	ENSP00000495993.1:p.Ser55=
ENST00000300589.6:c.246C=	ENSP00000300589.2:p.Ser82=
ENST00000526417.6:n.233C=
ENST00000527070.5:c.*861C=	ENSP00000435149.1:n.*861C=
ENST00000531674.1:c.165C=	ENSP00000431681.1:p.Ser55=
ENST00000532206.1:n.350C=
NM_001293557.1:c.165C=	NP_001280486.1:p.Ser55=
NM_022162.2:c.246C=	NP_071445.1:p.Ser82=
XM_005256084.2:c.165C=	XP_005256141.1:p.Ser55=
XM_006721242.2:c.165C=	XP_006721305.1:p.Ser55=
XM_006721243.2:c.165C=	XP_006721306.1:p.Ser55=
XM_011523258.1:c.-38+5998C=	XP_011521560.1:n.-38+5998C=
XM_011523259.1:c.-315C=	XP_011521561.1:n.-315C=
XM_011523260.1:c.165C=	XP_011521562.1:p.Ser55=
XM_011523261.1:c.165C=	XP_011521563.1:p.Ser55=
XR_429725.2:n.255C=
XR_429726.2:n.255C=
XR_933387.1:n.255C=
XM_005256084.4:c.165C=	XP_005256141.1:p.Ser55=
XM_006721242.4:c.165C=	XP_006721305.1:p.Ser55=
XM_006721243.4:c.165C=	XP_006721306.1:p.Ser55=
XM_011523259.2:c.-315C=	XP_011521561.1:n.-315C=
XM_011523260.3:c.165C=	XP_011521562.1:p.Ser55=
XM_011523261.2:c.165C=	XP_011521563.1:p.Ser55=
XM_017023536.1:c.-127+5998C=	XP_016879025.1:n.-127+5998C=
XM_017023537.1:c.-21+5998C=	XP_016879026.1:n.-21+5998C=
XR_429725.3:n.208C=
XR_429726.3:n.208C=
XR_933387.2:n.208C=
NM_001293557.2:c.165C=	NP_001280486.1:p.Ser55=
NM_001370466.1:c.165C= MANE Select	NP_001357395.1:p.Ser55=
NM_022162.3:c.246C=	NP_071445.1:p.Ser82=
NR_163434.1:n.230C=