Canonical Allele Identifier: CA381612200

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68153852T>G (hg19) ; chr11:g.68386384T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68386384T>G , CM000673.2:g.68386384T>G	GRCh38
NC_000011.9:g.68153852T>G , CM000673.1:g.68153852T>G	GRCh37
NC_000011.8:g.67910428T>G	NCBI36
NG_015835.1:g.78745T>G
NG_015835.2:g.78745T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1084T>G MANE Select	ENSP00000294304.6:p.Phe362Val
ENST00000294304.11:c.1084T>G	ENSP00000294304.6:p.Phe362Val
ENST00000529993.5:c.1084T>G	ENSP00000436652.1:p.Phe362Val
NM_001291902.1:c.-682T>G	NP_001278831.1:n.-682T>G
NM_002335.3:c.1084T>G	NP_002326.2:p.Phe362Val
XM_005273994.2:c.1084T>G	XP_005274051.1:p.Phe362Val
XM_011545029.1:c.1111T>G	XP_011543331.1:p.Phe371Val
XM_011545030.1:c.1111T>G	XP_011543332.1:p.Phe371Val
XM_011545031.1:c.1111T>G	XP_011543333.1:p.Phe371Val
XR_949925.1:n.1126T>G
XR_949926.1:n.1126T>G
XR_001747874.1:n.1126T>G
XR_949925.2:n.1126T>G
XR_949926.2:n.1126T>G
NM_002335.4:c.1084T>G MANE Select	NP_002326.2:p.Phe362Val
NM_001291902.2:c.-682T>G	NP_001278831.1:n.-682T>G