Canonical Allele Identifier: CA10638672

Gene: LRP4 LRP4-AS1

Linked Data

• ClinVar Variation Id: 304826
• ClinVar RCV Id: RCV000395858
• dbSNP Id: rs886048340
• MyVariant Identifiers: chr11:g.46878452dupA (hg19) ; chr11:g.46878451_46878452insA (hg19) ; chr11:g.46856901dupA (hg38) ; chr11:g.46856900_46856901insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46856901dup , CM000673.2:g.46856901dup	GRCh38
NC_000011.9:g.46878452dup , CM000673.1:g.46878452dup	GRCh37
NC_000011.8:g.46835028dup	NCBI36
NG_021394.1:g.66722dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378623.6:c.*2082dup (LRP4) MANE Select	ENSP00000367888.1:n.*2082dup
ENST00000378623.5:c.*2082dup (LRP4)	ENSP00000367888.1:n.*2082dup
ENST00000529604.1:n.2743dup (LRP4)
NM_002334.3:c.*2082dup (LRP4)	NP_002325.2:n.*2082dup
NR_038909.1:n.197+10184dup (LRP4-AS1)
XM_011520102.1:c.*2082dup (LRP4)	XP_011518404.1:n.*2082dup
XM_011520103.1:c.*2082dup (LRP4)	XP_011518405.1:n.*2082dup
XM_011520104.1:c.*2082dup (LRP4)	XP_011518406.1:n.*2082dup
XM_011520103.2:c.*2082dup (LRP4)	XP_011518405.1:n.*2082dup
XM_011520104.2:c.*2082dup (LRP4)	XP_011518406.1:n.*2082dup
NM_002334.4:c.*2082dup (LRP4) MANE Select	NP_002325.2:n.*2082dup