Canonical Allele Identifier: CA381616635

Gene: LRP5

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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