Canonical Allele Identifier: CA1980629502

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68347861_68347865delinsCTATT , CM000673.2:g.68347861_68347865delinsCTATT	GRCh38
NC_000011.9:g.68115329_68115333delinsCTATT , CM000673.1:g.68115329_68115333delinsCTATT	GRCh37
NC_000011.8:g.67871905_67871909delinsCTATT	NCBI36
NG_015835.1:g.40222_40226delinsCTATT
NG_015835.2:g.40222_40226delinsCTATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.106_110delinsCTATT MANE Select	ENSP00000294304.6:p.Leu36=
ENST00000294304.11:c.106_110delinsCTATT	ENSP00000294304.6:p.Leu36=
ENST00000529993.5:c.106_110delinsCTATT	ENSP00000436652.1:p.Leu36=
NM_001291902.1:c.-1660_-1656delinsCTATT	NP_001278831.1:n.-1660_-1656delinsCTATT
NM_002335.3:c.106_110delinsCTATT	NP_002326.2:p.Leu36=
XM_005273994.2:c.106_110delinsCTATT	XP_005274051.1:p.Leu36=
XM_011545029.1:c.133_137delinsCTATT	XP_011543331.1:p.Leu45=
XM_011545030.1:c.133_137delinsCTATT	XP_011543332.1:p.Leu45=
XM_011545031.1:c.133_137delinsCTATT	XP_011543333.1:p.Leu45=
XR_949925.1:n.148_152delinsCTATT
XR_949926.1:n.148_152delinsCTATT
XR_001747874.1:n.148_152delinsCTATT
XR_949925.2:n.148_152delinsCTATT
XR_949926.2:n.148_152delinsCTATT
NM_002335.4:c.106_110delinsCTATT MANE Select	NP_002326.2:p.Leu36=
NM_001291902.2:c.-1660_-1656delinsCTATT	NP_001278831.1:n.-1660_-1656delinsCTATT