Canonical Allele Identifier: CA381610998

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68131264T>A (hg19) ; chr11:g.68363796T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68363796T>A , CM000673.2:g.68363796T>A	GRCh38
NC_000011.9:g.68131264T>A , CM000673.1:g.68131264T>A	GRCh37
NC_000011.8:g.67887840T>A	NCBI36
NG_015835.1:g.56157T>A
NG_015835.2:g.56157T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.736T>A MANE Select	ENSP00000294304.6:p.Ser246Thr
ENST00000294304.11:c.736T>A	ENSP00000294304.6:p.Ser246Thr
ENST00000529993.5:c.736T>A	ENSP00000436652.1:p.Ser246Thr
NM_001291902.1:c.-1030T>A	NP_001278831.1:n.-1030T>A
NM_002335.3:c.736T>A	NP_002326.2:p.Ser246Thr
XM_005273994.2:c.736T>A	XP_005274051.1:p.Ser246Thr
XM_011545029.1:c.763T>A	XP_011543331.1:p.Ser255Thr
XM_011545030.1:c.763T>A	XP_011543332.1:p.Ser255Thr
XM_011545031.1:c.763T>A	XP_011543333.1:p.Ser255Thr
XR_949925.1:n.778T>A
XR_949926.1:n.778T>A
XR_001747874.1:n.778T>A
XR_949925.2:n.778T>A
XR_949926.2:n.778T>A
NM_002335.4:c.736T>A MANE Select	NP_002326.2:p.Ser246Thr
NM_001291902.2:c.-1030T>A	NP_001278831.1:n.-1030T>A