Canonical Allele Identifier: CA2574901386

Gene: LRP5

Linked Data

• gnomAD v4: 11-68448723-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448723T>G , CM000673.2:g.68448723T>G	GRCh38
NC_000011.9:g.68216191T>G , CM000673.1:g.68216191T>G	GRCh37
NC_000011.8:g.67972767T>G	NCBI36
NG_015835.1:g.141084T>G
NG_015835.2:g.141084T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4587-86T>G MANE Select	ENSP00000294304.6:n.4587-86T>G
ENST00000294304.11:c.4587-86T>G	ENSP00000294304.6:n.4587-86T>G
ENST00000529481.1:n.178-86T>G
ENST00000529702.1:c.257-86T>G
ENST00000529993.5:c.*3193-86T>G	ENSP00000436652.1:n.*3193-86T>G
NM_001291902.1:c.2844-86T>G	NP_001278831.1:n.2844-86T>G
NM_002335.3:c.4587-86T>G	NP_002326.2:n.4587-86T>G
XM_005273994.2:c.4701-86T>G	XP_005274051.1:n.4701-86T>G
XM_011545029.1:c.4728-86T>G	XP_011543331.1:n.4728-86T>G
XM_011545030.1:c.4614-86T>G	XP_011543332.1:n.4614-86T>G
XM_011545031.1:c.4744-86T>G	XP_011543333.1:n.4744-86T>G
XR_949925.1:n.4974-86T>G
XR_949926.1:n.4990-86T>G
XM_017017735.1:c.2958-86T>G	XP_016873224.1:n.2958-86T>G
XM_017017736.1:c.2241-86T>G	XP_016873225.1:n.2241-86T>G
XR_949925.2:n.4974-86T>G
XR_949926.2:n.4990-86T>G
NM_002335.4:c.4587-86T>G MANE Select	NP_002326.2:n.4587-86T>G
NM_001291902.2:c.2844-86T>G	NP_001278831.1:n.2844-86T>G