Canonical Allele Identifier: CA381615665

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68174156C>A (hg19) ; chr11:g.68406688C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406688C>A , CM000673.2:g.68406688C>A	GRCh38
NC_000011.9:g.68174156C>A , CM000673.1:g.68174156C>A	GRCh37
NC_000011.8:g.67930732C>A	NCBI36
NG_015835.1:g.99049C>A
NG_015835.2:g.99049C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1966C>A MANE Select	ENSP00000294304.6:p.His656Asn
ENST00000294304.11:c.1966C>A	ENSP00000294304.6:p.His656Asn
ENST00000529993.5:c.*572C>A	ENSP00000436652.1:n.*572C>A
NM_001291902.1:c.223C>A	NP_001278831.1:p.His75Asn
NM_002335.3:c.1966C>A	NP_002326.2:p.His656Asn
XM_005273994.2:c.1966C>A	XP_005274051.1:p.His656Asn
XM_011545029.1:c.1993C>A	XP_011543331.1:p.His665Asn
XM_011545030.1:c.1993C>A	XP_011543332.1:p.His665Asn
XM_011545031.1:c.1993C>A	XP_011543333.1:p.His665Asn
XR_949925.1:n.2008C>A
XR_949926.1:n.2008C>A
XM_017017735.1:c.223C>A	XP_016873224.1:p.His75Asn
XR_001747874.1:n.2008C>A
XR_949925.2:n.2008C>A
XR_949926.2:n.2008C>A
NM_002335.4:c.1966C>A MANE Select	NP_002326.2:p.His656Asn
NM_001291902.2:c.223C>A	NP_001278831.1:p.His75Asn