Canonical Allele Identifier: CA381615326

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68174015A>C (hg19) ; chr11:g.68406547A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406547A>C , CM000673.2:g.68406547A>C	GRCh38
NC_000011.9:g.68174015A>C , CM000673.1:g.68174015A>C	GRCh37
NC_000011.8:g.67930591A>C	NCBI36
NG_015835.1:g.98908A>C
NG_015835.2:g.98908A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1825A>C MANE Select	ENSP00000294304.6:p.Asn609His
ENST00000294304.11:c.1825A>C	ENSP00000294304.6:p.Asn609His
ENST00000528890.1:n.464A>C
ENST00000529993.5:c.*431A>C	ENSP00000436652.1:n.*431A>C
NM_001291902.1:c.82A>C	NP_001278831.1:p.Asn28His
NM_002335.3:c.1825A>C	NP_002326.2:p.Asn609His
XM_005273994.2:c.1825A>C	XP_005274051.1:p.Asn609His
XM_011545029.1:c.1852A>C	XP_011543331.1:p.Asn618His
XM_011545030.1:c.1852A>C	XP_011543332.1:p.Asn618His
XM_011545031.1:c.1852A>C	XP_011543333.1:p.Asn618His
XR_949925.1:n.1867A>C
XR_949926.1:n.1867A>C
XM_017017735.1:c.82A>C	XP_016873224.1:p.Asn28His
XR_001747874.1:n.1867A>C
XR_949925.2:n.1867A>C
XR_949926.2:n.1867A>C
NM_002335.4:c.1825A>C MANE Select	NP_002326.2:p.Asn609His
NM_001291902.2:c.82A>C	NP_001278831.1:p.Asn28His