Canonical Allele Identifier: CA381610289

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68115432T>G (hg19) ; chr11:g.68347964T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68347964T>G , CM000673.2:g.68347964T>G	GRCh38
NC_000011.9:g.68115432T>G , CM000673.1:g.68115432T>G	GRCh37
NC_000011.8:g.67872008T>G	NCBI36
NG_015835.1:g.40325T>G
NG_015835.2:g.40325T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.209T>G MANE Select	ENSP00000294304.6:p.Phe70Cys
ENST00000294304.11:c.209T>G	ENSP00000294304.6:p.Phe70Cys
ENST00000529993.5:c.209T>G	ENSP00000436652.1:p.Phe70Cys
NM_001291902.1:c.-1557T>G	NP_001278831.1:n.-1557T>G
NM_002335.3:c.209T>G	NP_002326.2:p.Phe70Cys
XM_005273994.2:c.209T>G	XP_005274051.1:p.Phe70Cys
XM_011545029.1:c.236T>G	XP_011543331.1:p.Phe79Cys
XM_011545030.1:c.236T>G	XP_011543332.1:p.Phe79Cys
XM_011545031.1:c.236T>G	XP_011543333.1:p.Phe79Cys
XR_949925.1:n.251T>G
XR_949926.1:n.251T>G
XR_001747874.1:n.251T>G
XR_949925.2:n.251T>G
XR_949926.2:n.251T>G
NM_002335.4:c.209T>G MANE Select	NP_002326.2:p.Phe70Cys
NM_001291902.2:c.-1557T>G	NP_001278831.1:n.-1557T>G