Canonical Allele Identifier: CA10639230
Gene: LRP4 HGNC NCBI
LRP4-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304843
ClinVar RCV Id: RCV000380075
dbSNP Id: rs372674165
gnomAD v2: 11-46880490-A-G
gnomAD v3: 11-46858939-A-G
gnomAD v4: 11-46858939-A-G
MyVariant Identifiers: chr11:g.46880490A>G (hg19) chr11:g.46858939A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46858939A>G , CM000673.2:g.46858939A>G GRCh38
NC_000011.9:g.46880490A>G , CM000673.1:g.46880490A>G GRCh37
NC_000011.8:g.46837066A>G NCBI36
NG_021394.1:g.64684T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378623.6:c.*44T>C (LRP4) MANE Select ENSP00000367888.1:n.*44T>C
ENST00000378623.5:c.*44T>C (LRP4) ENSP00000367888.1:n.*44T>C
ENST00000529604.1:n.705T>C (LRP4)
NM_002334.3:c.*44T>C (LRP4) NP_002325.2:n.*44T>C
NR_038909.1:n.197+12222A>G (LRP4-AS1)
XM_011520102.1:c.*44T>C (LRP4) XP_011518404.1:n.*44T>C
XM_011520103.1:c.*44T>C (LRP4) XP_011518405.1:n.*44T>C
XM_011520104.1:c.*44T>C (LRP4) XP_011518406.1:n.*44T>C
XM_011520103.2:c.*44T>C (LRP4) XP_011518405.1:n.*44T>C
XM_011520104.2:c.*44T>C (LRP4) XP_011518406.1:n.*44T>C
NM_002334.4:c.*44T>C (LRP4) MANE Select NP_002325.2:n.*44T>C
Search 100 bp 5'
Search 100 bp 3'