Canonical Allele Identifier: CA1980629784

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68347964_68347965delinsTC , CM000673.2:g.68347964_68347965delinsTC	GRCh38
NC_000011.9:g.68115432_68115433delinsTC , CM000673.1:g.68115432_68115433delinsTC	GRCh37
NC_000011.8:g.67872008_67872009delinsTC	NCBI36
NG_015835.1:g.40325_40326delinsTC
NG_015835.2:g.40325_40326delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.209_210delinsTC MANE Select	ENSP00000294304.6:p.Phe70=
ENST00000294304.11:c.209_210delinsTC	ENSP00000294304.6:p.Phe70=
ENST00000529993.5:c.209_210delinsTC	ENSP00000436652.1:p.Phe70=
NM_001291902.1:c.-1557_-1556delinsTC	NP_001278831.1:n.-1557_-1556delinsTC
NM_002335.3:c.209_210delinsTC	NP_002326.2:p.Phe70=
XM_005273994.2:c.209_210delinsTC	XP_005274051.1:p.Phe70=
XM_011545029.1:c.236_237delinsTC	XP_011543331.1:p.Phe79=
XM_011545030.1:c.236_237delinsTC	XP_011543332.1:p.Phe79=
XM_011545031.1:c.236_237delinsTC	XP_011543333.1:p.Phe79=
XR_949925.1:n.251_252delinsTC
XR_949926.1:n.251_252delinsTC
XR_001747874.1:n.251_252delinsTC
XR_949925.2:n.251_252delinsTC
XR_949926.2:n.251_252delinsTC
NM_002335.4:c.209_210delinsTC MANE Select	NP_002326.2:p.Phe70=
NM_001291902.2:c.-1557_-1556delinsTC	NP_001278831.1:n.-1557_-1556delinsTC