Canonical Allele Identifier: CA380284078

Gene: LRP4 LRP4-AS1

Linked Data

• ClinVar Variation Id: 2163296
• ClinVar RCV Id: RCV003092247
• MyVariant Identifiers: chr11:g.46880746G>A (hg19) ; chr11:g.46859195G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46859195G>A , CM000673.2:g.46859195G>A	GRCh38
NC_000011.9:g.46880746G>A , CM000673.1:g.46880746G>A	GRCh37
NC_000011.8:g.46837322G>A	NCBI36
NG_021394.1:g.64428C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378623.6:c.5506C>T (LRP4) MANE Select	ENSP00000367888.1:p.Leu1836Phe
ENST00000378623.5:c.5506C>T (LRP4)	ENSP00000367888.1:p.Leu1836Phe
ENST00000529604.1:n.449C>T (LRP4)
NM_002334.3:c.5506C>T (LRP4)	NP_002325.2:p.Leu1836Phe
NR_038909.1:n.197+12478G>A (LRP4-AS1)
XM_011520102.1:c.5719C>T (LRP4)	XP_011518404.1:p.Leu1907Phe
XM_011520103.1:c.4702C>T (LRP4)	XP_011518405.1:p.Leu1568Phe
XM_011520104.1:c.3271C>T (LRP4)	XP_011518406.1:p.Leu1091Phe
XM_011520103.2:c.4702C>T (LRP4)	XP_011518405.1:p.Leu1568Phe
XM_011520104.2:c.3271C>T (LRP4)	XP_011518406.1:p.Leu1091Phe
NM_002334.4:c.5506C>T (LRP4) MANE Select	NP_002325.2:p.Leu1836Phe