Canonical Allele Identifier: CA1697721891

Gene: NOD1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30446094A= , CM000669.2:g.30446094A=	GRCh38
NC_000007.13:g.30485710A= , CM000669.1:g.30485710A=	GRCh37
NC_000007.12:g.30452235A=	NCBI36
NG_013025.1:g.37684T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006092.4:c.2453+47T= MANE Select	NP_006083.1:n.2453+47T=
ENST00000222823.9:c.2453+47T= MANE Select	ENSP00000222823.4:n.2453+47T=
NM_001354849.1:c.2453+47T=	NP_001341778.1:n.2453+47T=
NM_001354849.2:c.2453+47T=	NP_001341778.1:n.2453+47T=
NM_006092.2:c.2453+47T=	NP_006083.1:n.2453+47T=
NM_006092.3:c.2453+47T=	NP_006083.1:n.2453+47T=
NR_149002.1:n.3115+47T=
NR_149002.2:n.3033+47T=
ENST00000222823.8:c.2453+47T=	ENSP00000222823.4:n.2453+47T=
ENST00000434755.5:c.*163+47T=	ENSP00000416946.1:n.*163+47T=
ENST00000489614.5:n.1837+47T=
XM_005249568.1:c.2453+47T=	XP_005249625.1:n.2453+47T=
XM_005249572.1:c.2453+47T=	XP_005249629.1:n.2453+47T=
XM_005249576.1:c.1709+47T=	XP_005249633.1:n.1709+47T=
XM_006715633.2:c.2453+47T=	XP_006715696.1:n.2453+47T=
XM_011515079.1:c.2453+47T=	XP_011513381.1:n.2453+47T=
XM_011515080.1:c.2453+47T=	XP_011513382.1:n.2453+47T=
XM_011515080.2:c.2453+47T=	XP_011513382.1:n.2453+47T=
XM_011515081.1:c.2453+47T=	XP_011513383.1:n.2453+47T=
XM_011515081.2:c.2453+47T=	XP_011513383.1:n.2453+47T=
XM_011515082.1:c.2453+47T=	XP_011513384.1:n.2453+47T=
XM_011515083.1:c.2405+47T=	XP_011513385.1:n.2405+47T=
XM_011515084.1:c.2453+47T=	XP_011513386.1:n.2453+47T=
XM_011515085.1:c.2453+47T=	XP_011513387.1:n.2453+47T=
XM_011515086.1:c.2453+47T=	XP_011513388.1:n.2453+47T=
XM_011515087.1:c.2453+47T=	XP_011513389.1:n.2453+47T=
XM_017011674.1:c.2453+47T=	XP_016867163.1:n.2453+47T=
XR_001744529.1:n.3031+47T=
XR_002956406.1:n.4968+47T=
XR_926907.1:n.3031+47T=
XR_926908.2:n.3081+47T=