Canonical Allele Identifier: CA230161

Gene: NLRX1

Linked Data

• ClinVar Variation Id: 103130
• ClinVar RCV Id: RCV000089390
• dbSNP Id: rs199476032
• ExAC: 11:119042066 A / G
• gnomAD v2: 11-119042066-A-G
• gnomAD v3: 11-119171357-A-G
• gnomAD v4: 11-119171357-A-G
• MyVariant Identifiers: chr11:g.119042066A>G (hg19) ; chr11:g.119171357A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119171357A>G , CM000673.2:g.119171357A>G	GRCh38
NC_000011.9:g.119042066A>G , CM000673.1:g.119042066A>G	GRCh37
NC_000011.8:g.118547276A>G	NCBI36
NG_047185.1:g.8024A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474751.7:c.-511A>G	ENSP00000516518.1:n.-511A>G
ENST00000706727.1:c.-47A>G	ENSP00000516516.1:n.-47A>G
ENST00000706728.1:c.-511A>G	ENSP00000516517.1:n.-511A>G
ENST00000706729.1:c.-47A>G	ENSP00000516519.1:n.-47A>G
ENST00000409109.6:c.-47A>G MANE Select	ENSP00000387334.1:n.-47A>G
ENST00000292199.6:c.-47A>G	ENSP00000292199.2:n.-47A>G
ENST00000409109.5:c.-47A>G	ENSP00000387334.1:n.-47A>G
ENST00000409265.8:c.-47A>G	ENSP00000386858.5:n.-47A>G
ENST00000409991.5:c.-47A>G	ENSP00000386851.1:n.-47A>G
ENST00000422249.5:c.-47A>G	ENSP00000402381.1:n.-47A>G
ENST00000449394.5:c.-47A>G	ENSP00000402801.1:n.-47A>G
ENST00000454811.5:c.-47A>G	ENSP00000400268.1:n.-47A>G
ENST00000468765.1:n.158A>G
ENST00000474751.6:n.332A>G
ENST00000481860.6:n.155A>G
ENST00000482180.5:n.101A>G
ENST00000525863.1:c.-47A>G	ENSP00000433442.1:n.-47A>G
NM_001282143.1:c.-47A>G	NP_001269072.1:n.-47A>G
NM_001282144.1:c.-47A>G	NP_001269073.1:n.-47A>G
NM_001282358.1:c.-47A>G	NP_001269287.1:n.-47A>G
NM_024618.3:c.-47A>G	NP_078894.2:n.-47A>G
XM_005271669.1:c.-47A>G	XP_005271726.1:n.-47A>G
XM_005271670.1:c.-511A>G	XP_005271727.1:n.-511A>G
XM_005271671.1:c.-511A>G	XP_005271728.1:n.-511A>G
XM_005271672.1:c.-511A>G	XP_005271729.1:n.-511A>G
XM_006718904.1:c.-47A>G	XP_006718967.1:n.-47A>G
XM_011542980.1:c.-47A>G	XP_011541282.1:n.-47A>G
XM_017018294.2:c.-47A>G	XP_016873783.1:n.-47A>G
NM_001282144.2:c.-47A>G MANE Select	NP_001269073.1:n.-47A>G
NM_001282143.2:c.-47A>G	NP_001269072.1:n.-47A>G
NM_024618.4:c.-47A>G	NP_078894.2:n.-47A>G
NM_001282358.2:c.-47A>G	NP_001269287.1:n.-47A>G