Canonical Allele Identifier: CA1980610849

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68426052T= , CM000673.2:g.68426052T=	GRCh38
NC_000011.9:g.68193520T= , CM000673.1:g.68193520T=	GRCh37
NC_000011.8:g.67950096T=	NCBI36
NG_015835.1:g.118413T=
NG_015835.2:g.118413T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.3502T= MANE Select	ENSP00000294304.6:p.Tyr1168=
ENST00000294304.11:c.3502T=	ENSP00000294304.6:p.Tyr1168=
ENST00000529993.5:c.*2108T=	ENSP00000436652.1:n.*2108T=
NM_001291902.1:c.1759T=	NP_001278831.1:p.Tyr587=
NM_002335.3:c.3502T=	NP_002326.2:p.Tyr1168=
XM_005273994.2:c.3502T=	XP_005274051.1:p.Tyr1168=
XM_011545029.1:c.3529T=	XP_011543331.1:p.Tyr1177=
XM_011545030.1:c.3529T=	XP_011543332.1:p.Tyr1177=
XM_011545031.1:c.3529T=	XP_011543333.1:p.Tyr1177=
XR_949925.1:n.3544T=
XR_949926.1:n.3544T=
XM_017017735.1:c.1759T=	XP_016873224.1:p.Tyr587=
XM_017017736.1:c.1042T=	XP_016873225.1:p.Tyr348=
XR_949925.2:n.3544T=
XR_949926.2:n.3544T=
NM_002335.4:c.3502T= MANE Select	NP_002326.2:p.Tyr1168=
NM_001291902.2:c.1759T=	NP_001278831.1:p.Tyr587=