Canonical Allele Identifier: CA381616633

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68177559T>A (hg19) ; chr11:g.68410091T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68410091T>A , CM000673.2:g.68410091T>A	GRCh38
NC_000011.9:g.68177559T>A , CM000673.1:g.68177559T>A	GRCh37
NC_000011.8:g.67934135T>A	NCBI36
NG_015835.1:g.102452T>A
NG_015835.2:g.102452T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.2269T>A MANE Select	ENSP00000294304.6:p.Trp757Arg
ENST00000294304.11:c.2269T>A	ENSP00000294304.6:p.Trp757Arg
ENST00000528714.1:n.63T>A
ENST00000529993.5:c.*875T>A	ENSP00000436652.1:n.*875T>A
NM_001291902.1:c.526T>A	NP_001278831.1:p.Trp176Arg
NM_002335.3:c.2269T>A	NP_002326.2:p.Trp757Arg
XM_005273994.2:c.2269T>A	XP_005274051.1:p.Trp757Arg
XM_011545029.1:c.2296T>A	XP_011543331.1:p.Trp766Arg
XM_011545030.1:c.2296T>A	XP_011543332.1:p.Trp766Arg
XM_011545031.1:c.2296T>A	XP_011543333.1:p.Trp766Arg
XR_949925.1:n.2311T>A
XR_949926.1:n.2311T>A
XM_017017735.1:c.526T>A	XP_016873224.1:p.Trp176Arg
XR_001747874.1:n.2311T>A
XR_949925.2:n.2311T>A
XR_949926.2:n.2311T>A
NM_002335.4:c.2269T>A MANE Select	NP_002326.2:p.Trp757Arg
NM_001291902.2:c.526T>A	NP_001278831.1:p.Trp176Arg