Canonical Allele Identifier: CA6149467
Gene: LRP5 HGNC NCBI

Linked Data

dbSNP Id: rs754464622

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68406545G>A , CM000673.2:g.68406545G>A GRCh38
NC_000011.9:g.68174013G>A , CM000673.1:g.68174013G>A GRCh37
NC_000011.8:g.67930589G>A NCBI36
NG_015835.1:g.98906G>A
NG_015835.2:g.98906G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1823G>A MANE Select ENSP00000294304.6:p.Arg608Lys
ENST00000294304.11:c.1823G>A ENSP00000294304.6:p.Arg608Lys
ENST00000528890.1:n.462G>A
ENST00000529993.5:c.*429G>A ENSP00000436652.1:n.*429G>A
NM_001291902.1:c.80G>A NP_001278831.1:p.Arg27Lys
NM_002335.3:c.1823G>A NP_002326.2:p.Arg608Lys
XM_005273994.2:c.1823G>A XP_005274051.1:p.Arg608Lys
XM_011545029.1:c.1850G>A XP_011543331.1:p.Arg617Lys
XM_011545030.1:c.1850G>A XP_011543332.1:p.Arg617Lys
XM_011545031.1:c.1850G>A XP_011543333.1:p.Arg617Lys
XR_949925.1:n.1865G>A
XR_949926.1:n.1865G>A
XM_017017735.1:c.80G>A XP_016873224.1:p.Arg27Lys
XR_001747874.1:n.1865G>A
XR_949925.2:n.1865G>A
XR_949926.2:n.1865G>A
NM_002335.4:c.1823G>A MANE Select NP_002326.2:p.Arg608Lys
NM_001291902.2:c.80G>A NP_001278831.1:p.Arg27Lys