Canonical Allele Identifier: CA381613788

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68201172A>C (hg19) ; chr11:g.68433704A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68433704A>C , CM000673.2:g.68433704A>C	GRCh38
NC_000011.9:g.68201172A>C , CM000673.1:g.68201172A>C	GRCh37
NC_000011.8:g.67957748A>C	NCBI36
NG_015835.1:g.126065A>C
NG_015835.2:g.126065A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.3866A>C MANE Select	ENSP00000294304.6:p.Gln1289Pro
ENST00000294304.11:c.3866A>C	ENSP00000294304.6:p.Gln1289Pro
ENST00000529993.5:c.*2472A>C	ENSP00000436652.1:n.*2472A>C
NM_001291902.1:c.2123A>C	NP_001278831.1:p.Gln708Pro
NM_002335.3:c.3866A>C	NP_002326.2:p.Gln1289Pro
XM_005273994.2:c.3866A>C	XP_005274051.1:p.Gln1289Pro
XM_011545029.1:c.3893A>C	XP_011543331.1:p.Gln1298Pro
XM_011545030.1:c.3893A>C	XP_011543332.1:p.Gln1298Pro
XM_011545031.1:c.3893A>C	XP_011543333.1:p.Gln1298Pro
XR_949925.1:n.3908A>C
XR_949926.1:n.3908A>C
XM_017017735.1:c.2123A>C	XP_016873224.1:p.Gln708Pro
XM_017017736.1:c.1406A>C	XP_016873225.1:p.Gln469Pro
XR_949925.2:n.3908A>C
XR_949926.2:n.3908A>C
NM_002335.4:c.3866A>C MANE Select	NP_002326.2:p.Gln1289Pro
NM_001291902.2:c.2123A>C	NP_001278831.1:p.Gln708Pro