Canonical Allele Identifier: CA1697700388

Gene: NOD1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30433407C= , CM000669.2:g.30433407C=	GRCh38
NC_000007.13:g.30473023C= , CM000669.1:g.30473023C=	GRCh37
NC_000007.12:g.30439548C=	NCBI36
NG_013025.1:g.50371G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222823.9:c.2622-228G= MANE Select	ENSP00000222823.4:n.2622-228G=
ENST00000222823.8:c.2622-228G=	ENSP00000222823.4:n.2622-228G=
ENST00000434755.5:c.*332-228G=	ENSP00000416946.1:n.*332-228G=
ENST00000467706.1:n.8G=
ENST00000489614.5:n.1838-3950G=
NM_006092.2:c.2622-228G=	NP_006083.1:n.2622-228G=
XM_005249568.1:c.2622-228G=	XP_005249625.1:n.2622-228G=
XM_005249572.1:c.2622-228G=	XP_005249629.1:n.2622-228G=
XM_005249576.1:c.1878-228G=	XP_005249633.1:n.1878-228G=
XM_006715633.2:c.2622-228G=	XP_006715696.1:n.2622-228G=
XM_011515079.1:c.2622-228G=	XP_011513381.1:n.2622-228G=
XM_011515080.1:c.2622-228G=	XP_011513382.1:n.2622-228G=
XM_011515081.1:c.2622-228G=	XP_011513383.1:n.2622-228G=
XM_011515082.1:c.2619-228G=	XP_011513384.1:n.2619-228G=
XM_011515083.1:c.2574-228G=	XP_011513385.1:n.2574-228G=
XM_011515084.1:c.2538-228G=	XP_011513386.1:n.2538-228G=
XM_011515085.1:c.2454-3950G=	XP_011513387.1:n.2454-3950G=
XM_011515086.1:c.2454-7697G=	XP_011513388.1:n.2454-7697G=
XR_926907.1:n.3200-228G=
NM_001354849.1:c.2538-228G=	NP_001341778.1:n.2538-228G=
NM_006092.3:c.2622-228G=	NP_006083.1:n.2622-228G=
NR_149002.1:n.3284-228G=
XM_011515080.2:c.2622-228G=	XP_011513382.1:n.2622-228G=
XM_011515081.2:c.2622-228G=	XP_011513383.1:n.2622-228G=
XM_017011674.1:c.2622-228G=	XP_016867163.1:n.2622-228G=
XR_002956406.1:n.4969-3950G=
XR_926908.2:n.3250-228G=
NM_006092.4:c.2622-228G= MANE Select	NP_006083.1:n.2622-228G=
NM_001354849.2:c.2538-228G=	NP_001341778.1:n.2538-228G=
NR_149002.2:n.3202-228G=