Canonical Allele Identifier: CA381611843

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68125219C>A (hg19) ; chr11:g.68357751C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68357751C>A , CM000673.2:g.68357751C>A	GRCh38
NC_000011.9:g.68125219C>A , CM000673.1:g.68125219C>A	GRCh37
NC_000011.8:g.67881795C>A	NCBI36
NG_015835.1:g.50112C>A
NG_015835.2:g.50112C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.590C>A MANE Select	ENSP00000294304.6:p.Pro197His
ENST00000294304.11:c.590C>A	ENSP00000294304.6:p.Pro197His
ENST00000529993.5:c.590C>A	ENSP00000436652.1:p.Pro197His
NM_001291902.1:c.-1176C>A	NP_001278831.1:n.-1176C>A
NM_002335.3:c.590C>A	NP_002326.2:p.Pro197His
XM_005273994.2:c.590C>A	XP_005274051.1:p.Pro197His
XM_011545029.1:c.617C>A	XP_011543331.1:p.Pro206His
XM_011545030.1:c.617C>A	XP_011543332.1:p.Pro206His
XM_011545031.1:c.617C>A	XP_011543333.1:p.Pro206His
XR_949925.1:n.632C>A
XR_949926.1:n.632C>A
XR_001747874.1:n.632C>A
XR_949925.2:n.632C>A
XR_949926.2:n.632C>A
NM_002335.4:c.590C>A MANE Select	NP_002326.2:p.Pro197His
NM_001291902.2:c.-1176C>A	NP_001278831.1:n.-1176C>A