Canonical Allele Identifier: CA454518522

Gene: NOD1

Linked Data

• MyVariant Identifiers: chr7:g.30492250T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30452634T>A , CM000669.2:g.30452634T>A	GRCh38
NC_000007.13:g.30492250T>A , CM000669.1:g.30492250T>A	GRCh37
NC_000007.12:g.30458775T>A	NCBI36
NG_013025.1:g.31144A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222823.9:c.783A>T MANE Select	ENSP00000222823.4:p.Pro261=
ENST00000222823.8:c.783A>T	ENSP00000222823.4:p.Pro261=
ENST00000434755.5:c.783A>T	ENSP00000416946.1:p.Pro261=
NM_006092.2:c.783A>T	NP_006083.1:p.Pro261=
XM_005249568.1:c.783A>T	XP_005249625.1:p.Pro261=
XM_005249572.1:c.783A>T	XP_005249629.1:p.Pro261=
XM_005249576.1:c.39A>T	XP_005249633.1:p.Pro13=
XM_006715633.2:c.783A>T	XP_006715696.1:p.Pro261=
XM_011515079.1:c.783A>T	XP_011513381.1:p.Pro261=
XM_011515080.1:c.783A>T	XP_011513382.1:p.Pro261=
XM_011515081.1:c.783A>T	XP_011513383.1:p.Pro261=
XM_011515082.1:c.783A>T	XP_011513384.1:p.Pro261=
XM_011515083.1:c.783A>T	XP_011513385.1:p.Pro261=
XM_011515084.1:c.783A>T	XP_011513386.1:p.Pro261=
XM_011515085.1:c.783A>T	XP_011513387.1:p.Pro261=
XM_011515086.1:c.783A>T	XP_011513388.1:p.Pro261=
XM_011515087.1:c.783A>T	XP_011513389.1:p.Pro261=
XM_011515088.1:c.783A>T	XP_011513390.1:p.Pro261=
XR_926907.1:n.1361A>T
XR_926908.1:n.1361A>T
XR_926909.1:n.1361A>T
XR_926910.1:n.1361A>T
NM_001354849.1:c.783A>T	NP_001341778.1:p.Pro261=
NM_006092.3:c.783A>T	NP_006083.1:p.Pro261=
NR_149002.1:n.1395A>T
XM_011515080.2:c.783A>T	XP_011513382.1:p.Pro261=
XM_011515081.2:c.783A>T	XP_011513383.1:p.Pro261=
XM_011515088.2:c.783A>T	XP_011513390.1:p.Pro261=
XM_017011674.1:c.783A>T	XP_016867163.1:p.Pro261=
XR_001744529.1:n.1361A>T
XR_001744530.1:n.1361A>T
XR_002956406.1:n.1309A>T
XR_926908.2:n.1361A>T
XR_926909.2:n.1361A>T
NM_006092.4:c.783A>T MANE Select	NP_006083.1:p.Pro261=
NM_001354849.2:c.783A>T	NP_001341778.1:p.Pro261=
NR_149002.2:n.1313A>T