Canonical Allele Identifier: CA381612073

Gene: LRP5

Linked Data

• ClinVar Variation Id: 2706567
• ClinVar RCV Id: RCV003552050
• MyVariant Identifiers: chr11:g.68153784G>T (hg19) ; chr11:g.68386316G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68386316G>T , CM000673.2:g.68386316G>T	GRCh38
NC_000011.9:g.68153784G>T , CM000673.1:g.68153784G>T	GRCh37
NC_000011.8:g.67910360G>T	NCBI36
NG_015835.1:g.78677G>T
NG_015835.2:g.78677G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1016G>T MANE Select	ENSP00000294304.6:p.Gly339Val
ENST00000294304.11:c.1016G>T	ENSP00000294304.6:p.Gly339Val
ENST00000529993.5:c.1016G>T	ENSP00000436652.1:p.Gly339Val
NM_001291902.1:c.-750G>T	NP_001278831.1:n.-750G>T
NM_002335.3:c.1016G>T	NP_002326.2:p.Gly339Val
XM_005273994.2:c.1016G>T	XP_005274051.1:p.Gly339Val
XM_011545029.1:c.1043G>T	XP_011543331.1:p.Gly348Val
XM_011545030.1:c.1043G>T	XP_011543332.1:p.Gly348Val
XM_011545031.1:c.1043G>T	XP_011543333.1:p.Gly348Val
XR_949925.1:n.1058G>T
XR_949926.1:n.1058G>T
XR_001747874.1:n.1058G>T
XR_949925.2:n.1058G>T
XR_949926.2:n.1058G>T
NM_002335.4:c.1016G>T MANE Select	NP_002326.2:p.Gly339Val
NM_001291902.2:c.-750G>T	NP_001278831.1:n.-750G>T