Canonical Allele Identifier: CA381616702

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68177589G>A (hg19) ; chr11:g.68410121G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68410121G>A , CM000673.2:g.68410121G>A	GRCh38
NC_000011.9:g.68177589G>A , CM000673.1:g.68177589G>A	GRCh37
NC_000011.8:g.67934165G>A	NCBI36
NG_015835.1:g.102482G>A
NG_015835.2:g.102482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.2299G>A MANE Select	ENSP00000294304.6:p.Ala767Thr
ENST00000294304.11:c.2299G>A	ENSP00000294304.6:p.Ala767Thr
ENST00000528714.1:n.93G>A
ENST00000529993.5:c.*905G>A	ENSP00000436652.1:n.*905G>A
NM_001291902.1:c.556G>A	NP_001278831.1:p.Ala186Thr
NM_002335.3:c.2299G>A	NP_002326.2:p.Ala767Thr
XM_005273994.2:c.2299G>A	XP_005274051.1:p.Ala767Thr
XM_011545029.1:c.2326G>A	XP_011543331.1:p.Ala776Thr
XM_011545030.1:c.2326G>A	XP_011543332.1:p.Ala776Thr
XM_011545031.1:c.2326G>A	XP_011543333.1:p.Ala776Thr
XR_949925.1:n.2341G>A
XR_949926.1:n.2341G>A
XM_017017735.1:c.556G>A	XP_016873224.1:p.Ala186Thr
XR_001747874.1:n.2341G>A
XR_949925.2:n.2341G>A
XR_949926.2:n.2341G>A
NM_002335.4:c.2299G>A MANE Select	NP_002326.2:p.Ala767Thr
NM_001291902.2:c.556G>A	NP_001278831.1:p.Ala186Thr