Canonical Allele Identifier: CA475462502

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68216290C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448822C>A , CM000673.2:g.68448822C>A	GRCh38
NC_000011.9:g.68216290C>A , CM000673.1:g.68216290C>A	GRCh37
NC_000011.8:g.67972866C>A	NCBI36
NG_015835.1:g.141183C>A
NG_015835.2:g.141183C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4600C>A MANE Select	ENSP00000294304.6:p.Arg1534=
ENST00000294304.11:c.4600C>A	ENSP00000294304.6:p.Arg1534=
ENST00000529481.1:n.191C>A
ENST00000529702.1:c.270C>A
ENST00000529993.5:c.*3206C>A	ENSP00000436652.1:n.*3206C>A
NM_001291902.1:c.2857C>A	NP_001278831.1:p.Arg953=
NM_002335.3:c.4600C>A	NP_002326.2:p.Arg1534=
XM_005273994.2:c.4714C>A	XP_005274051.1:p.Arg1572=
XM_011545029.1:c.4741C>A	XP_011543331.1:p.Arg1581=
XM_011545030.1:c.4627C>A	XP_011543332.1:p.Arg1543=
XM_011545031.1:c.4757C>A	XP_011543333.1:p.Ser1586Ter
XR_949925.1:n.4987C>A
XR_949926.1:n.5003C>A
XM_017017735.1:c.2971C>A	XP_016873224.1:p.Arg991=
XM_017017736.1:c.2254C>A	XP_016873225.1:p.Arg752=
XR_949925.2:n.4987C>A
XR_949926.2:n.5003C>A
NM_002335.4:c.4600C>A MANE Select	NP_002326.2:p.Arg1534=
NM_001291902.2:c.2857C>A	NP_001278831.1:p.Arg953=