Canonical Allele Identifier: CA2574901390

Gene: LRP5

Linked Data

• gnomAD v4: 11-68448743-GGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448748_68448750del , CM000673.2:g.68448748_68448750del	GRCh38
NC_000011.9:g.68216216_68216218del , CM000673.1:g.68216216_68216218del	GRCh37
NC_000011.8:g.67972792_67972794del	NCBI36
NG_015835.1:g.141109_141111del
NG_015835.2:g.141109_141111del

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4587-61_4587-59del MANE Select	ENSP00000294304.6:n.4587-61_4587-59del
ENST00000294304.11:c.4587-61_4587-59del	ENSP00000294304.6:n.4587-61_4587-59del
ENST00000529481.1:n.178-61_178-59del
ENST00000529702.1:c.257-61_257-59del
ENST00000529993.5:c.*3193-61_*3193-59del	ENSP00000436652.1:n.*3193-61_*3193-59del
NM_001291902.1:c.2844-61_2844-59del	NP_001278831.1:n.2844-61_2844-59del
NM_002335.3:c.4587-61_4587-59del	NP_002326.2:n.4587-61_4587-59del
XM_005273994.2:c.4701-61_4701-59del	XP_005274051.1:n.4701-61_4701-59del
XM_011545029.1:c.4728-61_4728-59del	XP_011543331.1:n.4728-61_4728-59del
XM_011545030.1:c.4614-61_4614-59del	XP_011543332.1:n.4614-61_4614-59del
XM_011545031.1:c.4744-61_4744-59del	XP_011543333.1:n.4744-61_4744-59del
XR_949925.1:n.4974-61_4974-59del
XR_949926.1:n.4990-61_4990-59del
XM_017017735.1:c.2958-61_2958-59del	XP_016873224.1:n.2958-61_2958-59del
XM_017017736.1:c.2241-61_2241-59del	XP_016873225.1:n.2241-61_2241-59del
XR_949925.2:n.4974-61_4974-59del
XR_949926.2:n.4990-61_4990-59del
NM_002335.4:c.4587-61_4587-59del MANE Select	NP_002326.2:n.4587-61_4587-59del
NM_001291902.2:c.2844-61_2844-59del	NP_001278831.1:n.2844-61_2844-59del