Canonical Allele Identifier: CA2614716782

Gene: LRP5

Linked Data

• gnomAD v4: 11-68446320-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68446323del , CM000673.2:g.68446323del	GRCh38
NC_000011.9:g.68213791del , CM000673.1:g.68213791del	GRCh37
NC_000011.8:g.67970367del	NCBI36
NG_015835.1:g.138684del
NG_015835.2:g.138684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.4489-113del MANE Select	ENSP00000294304.6:n.4489-113del
ENST00000294304.11:c.4489-113del	ENSP00000294304.6:n.4489-113del
ENST00000529702.1:c.159-113del
ENST00000529993.5:c.*3095-113del	ENSP00000436652.1:n.*3095-113del
NM_001291902.1:c.2746-113del	NP_001278831.1:n.2746-113del
NM_002335.3:c.4489-113del	NP_002326.2:n.4489-113del
XM_005273994.2:c.4603-113del	XP_005274051.1:n.4603-113del
XM_011545029.1:c.4630-113del	XP_011543331.1:n.4630-113del
XM_011545030.1:c.4516-113del	XP_011543332.1:n.4516-113del
XM_011545031.1:c.4646-113del	XP_011543333.1:n.4646-113del
XR_949925.1:n.4645-113del
XR_949926.1:n.4661-113del
XM_017017735.1:c.2860-113del	XP_016873224.1:n.2860-113del
XM_017017736.1:c.2143-113del	XP_016873225.1:n.2143-113del
XR_949925.2:n.4645-113del
XR_949926.2:n.4661-113del
NM_002335.4:c.4489-113del MANE Select	NP_002326.2:n.4489-113del
NM_001291902.2:c.2746-113del	NP_001278831.1:n.2746-113del