Canonical Allele Identifier: CA837495060

Gene: NOD1

Linked Data

• dbSNP Id: rs1277572652
• gnomAD v4: 7-30452299-C-CCCT
• MyVariant Identifiers: chr7:g.30491915_30491916insCCT (hg19) ; chr7:g.30452299_30452300insCCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30452299_30452300insCCT , CM000669.2:g.30452299_30452300insCCT	GRCh38
NC_000007.13:g.30491915_30491916insCCT , CM000669.1:g.30491915_30491916insCCT	GRCh37
NC_000007.12:g.30458440_30458441insCCT	NCBI36
NG_013025.1:g.31478_31479insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222823.9:c.1117_1118insAGG MANE Select	ENSP00000222823.4:p.Arg373delinsGlnGly
ENST00000222823.8:c.1117_1118insAGG	ENSP00000222823.4:p.Arg373delinsGlnGly
ENST00000434755.5:c.1117_1118insAGG	ENSP00000416946.1:p.Arg373delinsGlnGly
NM_006092.2:c.1117_1118insAGG	NP_006083.1:p.Arg373delinsGlnGly
XM_005249568.1:c.1117_1118insAGG	XP_005249625.1:p.Arg373delinsGlnGly
XM_005249572.1:c.1117_1118insAGG	XP_005249629.1:p.Arg373delinsGlnGly
XM_005249576.1:c.373_374insAGG	XP_005249633.1:p.Arg125delinsGlnGly
XM_006715633.2:c.1117_1118insAGG	XP_006715696.1:p.Arg373delinsGlnGly
XM_011515079.1:c.1117_1118insAGG	XP_011513381.1:p.Arg373delinsGlnGly
XM_011515080.1:c.1117_1118insAGG	XP_011513382.1:p.Arg373delinsGlnGly
XM_011515081.1:c.1117_1118insAGG	XP_011513383.1:p.Arg373delinsGlnGly
XM_011515082.1:c.1117_1118insAGG	XP_011513384.1:p.Arg373delinsGlnGly
XM_011515083.1:c.1117_1118insAGG	XP_011513385.1:p.Arg373delinsGlnGly
XM_011515084.1:c.1117_1118insAGG	XP_011513386.1:p.Arg373delinsGlnGly
XM_011515085.1:c.1117_1118insAGG	XP_011513387.1:p.Arg373delinsGlnGly
XM_011515086.1:c.1117_1118insAGG	XP_011513388.1:p.Arg373delinsGlnGly
XM_011515087.1:c.1117_1118insAGG	XP_011513389.1:p.Arg373delinsGlnGly
XM_011515088.1:c.1117_1118insAGG	XP_011513390.1:p.Arg373delinsGlnGly
XR_926907.1:n.1695_1696insAGG
XR_926908.1:n.1695_1696insAGG
XR_926909.1:n.1695_1696insAGG
XR_926910.1:n.1695_1696insAGG
NM_001354849.1:c.1117_1118insAGG	NP_001341778.1:p.Arg373delinsGlnGly
NM_006092.3:c.1117_1118insAGG	NP_006083.1:p.Arg373delinsGlnGly
NR_149002.1:n.1729_1730insAGG
XM_011515080.2:c.1117_1118insAGG	XP_011513382.1:p.Arg373delinsGlnGly
XM_011515081.2:c.1117_1118insAGG	XP_011513383.1:p.Arg373delinsGlnGly
XM_011515088.2:c.1117_1118insAGG	XP_011513390.1:p.Arg373delinsGlnGly
XM_017011674.1:c.1117_1118insAGG	XP_016867163.1:p.Arg373delinsGlnGly
XR_001744529.1:n.1695_1696insAGG
XR_001744530.1:n.1695_1696insAGG
XR_002956406.1:n.1643_1644insAGG
XR_926908.2:n.1695_1696insAGG
XR_926909.2:n.1695_1696insAGG
NM_006092.4:c.1117_1118insAGG MANE Select	NP_006083.1:p.Arg373delinsGlnGly
NM_001354849.2:c.1117_1118insAGG	NP_001341778.1:p.Arg373delinsGlnGly
NR_149002.2:n.1647_1648insAGG