Canonical Allele Identifier: CA381615631

Gene: LRP5

Linked Data

• dbSNP Id: rs756999448
• MyVariant Identifiers: chr11:g.68174138A>C (hg19) ; chr11:g.68406670A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68406670A>C , CM000673.2:g.68406670A>C	GRCh38
NC_000011.9:g.68174138A>C , CM000673.1:g.68174138A>C	GRCh37
NC_000011.8:g.67930714A>C	NCBI36
NG_015835.1:g.99031A>C
NG_015835.2:g.99031A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1948A>C MANE Select	ENSP00000294304.6:p.Thr650Pro
ENST00000294304.11:c.1948A>C	ENSP00000294304.6:p.Thr650Pro
ENST00000529993.5:c.*554A>C	ENSP00000436652.1:n.*554A>C
NM_001291902.1:c.205A>C	NP_001278831.1:p.Thr69Pro
NM_002335.3:c.1948A>C	NP_002326.2:p.Thr650Pro
XM_005273994.2:c.1948A>C	XP_005274051.1:p.Thr650Pro
XM_011545029.1:c.1975A>C	XP_011543331.1:p.Thr659Pro
XM_011545030.1:c.1975A>C	XP_011543332.1:p.Thr659Pro
XM_011545031.1:c.1975A>C	XP_011543333.1:p.Thr659Pro
XR_949925.1:n.1990A>C
XR_949926.1:n.1990A>C
XM_017017735.1:c.205A>C	XP_016873224.1:p.Thr69Pro
XR_001747874.1:n.1990A>C
XR_949925.2:n.1990A>C
XR_949926.2:n.1990A>C
NM_002335.4:c.1948A>C MANE Select	NP_002326.2:p.Thr650Pro
NM_001291902.2:c.205A>C	NP_001278831.1:p.Thr69Pro