Canonical Allele Identifier: CA1980609946

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68425226A= , CM000673.2:g.68425226A=	GRCh38
NC_000011.9:g.68192694A= , CM000673.1:g.68192694A=	GRCh37
NC_000011.8:g.67949270A=	NCBI36
NG_015835.1:g.117587A=
NG_015835.2:g.117587A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.3361A= MANE Select	ENSP00000294304.6:p.Asn1121=
ENST00000294304.11:c.3361A=	ENSP00000294304.6:p.Asn1121=
ENST00000529993.5:c.*1967A=	ENSP00000436652.1:n.*1967A=
NM_001291902.1:c.1618A=	NP_001278831.1:p.Asn540=
NM_002335.3:c.3361A=	NP_002326.2:p.Asn1121=
XM_005273994.2:c.3361A=	XP_005274051.1:p.Asn1121=
XM_011545029.1:c.3388A=	XP_011543331.1:p.Asn1130=
XM_011545030.1:c.3388A=	XP_011543332.1:p.Asn1130=
XM_011545031.1:c.3388A=	XP_011543333.1:p.Asn1130=
XR_949925.1:n.3403A=
XR_949926.1:n.3403A=
XM_017017735.1:c.1618A=	XP_016873224.1:p.Asn540=
XM_017017736.1:c.901A=	XP_016873225.1:p.Asn301=
XR_949925.2:n.3403A=
XR_949926.2:n.3403A=
NM_002335.4:c.3361A= MANE Select	NP_002326.2:p.Asn1121=
NM_001291902.2:c.1618A=	NP_001278831.1:p.Asn540=