Canonical Allele Identifier: CA679597914

Gene: LRP5

Linked Data

• dbSNP Id: rs1236549221
• gnomAD v3: 11-68446328-A-AG
• gnomAD v4: 11-68446328-A-AG
• MyVariant Identifiers: chr11:g.68213796_68213797insG (hg19) ; chr11:g.68446328_68446329insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68446334dup , CM000673.2:g.68446334dup	GRCh38
NC_000011.9:g.68213802dup , CM000673.1:g.68213802dup	GRCh37
NC_000011.8:g.67970378dup	NCBI36
NG_015835.1:g.138695dup
NG_015835.2:g.138695dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4489-102dup MANE Select	ENSP00000294304.6:n.4489-102dup
ENST00000294304.11:c.4489-102dup	ENSP00000294304.6:n.4489-102dup
ENST00000529702.1:c.159-102dup
ENST00000529993.5:c.*3095-102dup	ENSP00000436652.1:n.*3095-102dup
NM_001291902.1:c.2746-102dup	NP_001278831.1:n.2746-102dup
NM_002335.3:c.4489-102dup	NP_002326.2:n.4489-102dup
XM_005273994.2:c.4603-102dup	XP_005274051.1:n.4603-102dup
XM_011545029.1:c.4630-102dup	XP_011543331.1:n.4630-102dup
XM_011545030.1:c.4516-102dup	XP_011543332.1:n.4516-102dup
XM_011545031.1:c.4646-102dup	XP_011543333.1:n.4646-102dup
XR_949925.1:n.4645-102dup
XR_949926.1:n.4661-102dup
XM_017017735.1:c.2860-102dup	XP_016873224.1:n.2860-102dup
XM_017017736.1:c.2143-102dup	XP_016873225.1:n.2143-102dup
XR_949925.2:n.4645-102dup
XR_949926.2:n.4661-102dup
NM_002335.4:c.4489-102dup MANE Select	NP_002326.2:n.4489-102dup
NM_001291902.2:c.2746-102dup	NP_001278831.1:n.2746-102dup