Canonical Allele Identifier: CA676962464

Gene: LRP4 LRP4-AS1

Linked Data

• ClinVar Variation Id: 878015
• ClinVar RCV Id: RCV001104252
• dbSNP Id: rs1422186695
• gnomAD v3: 11-46858654-A-G
• gnomAD v4: 11-46858654-A-G
• MyVariant Identifiers: chr11:g.46880205A>G (hg19) ; chr11:g.46858654A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46858654A>G , CM000673.2:g.46858654A>G	GRCh38
NC_000011.9:g.46880205A>G , CM000673.1:g.46880205A>G	GRCh37
NC_000011.8:g.46836781A>G	NCBI36
NG_021394.1:g.64969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378623.6:c.*329T>C (LRP4) MANE Select	ENSP00000367888.1:n.*329T>C
ENST00000378623.5:c.*329T>C (LRP4)	ENSP00000367888.1:n.*329T>C
ENST00000529604.1:n.990T>C (LRP4)
NM_002334.3:c.*329T>C (LRP4)	NP_002325.2:n.*329T>C
NR_038909.1:n.197+11937A>G (LRP4-AS1)
XM_011520102.1:c.*329T>C (LRP4)	XP_011518404.1:n.*329T>C
XM_011520103.1:c.*329T>C (LRP4)	XP_011518405.1:n.*329T>C
XM_011520104.1:c.*329T>C (LRP4)	XP_011518406.1:n.*329T>C
XM_011520103.2:c.*329T>C (LRP4)	XP_011518405.1:n.*329T>C
XM_011520104.2:c.*329T>C (LRP4)	XP_011518406.1:n.*329T>C
NM_002334.4:c.*329T>C (LRP4) MANE Select	NP_002325.2:n.*329T>C