Canonical Allele Identifier: CA381610285

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68347963T>C , CM000673.2:g.68347963T>C	GRCh38
NC_000011.9:g.68115431T>C , CM000673.1:g.68115431T>C	GRCh37
NC_000011.8:g.67872007T>C	NCBI36
NG_015835.1:g.40324T>C
NG_015835.2:g.40324T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002335.4:c.208T>C MANE Select	NP_002326.2:p.Phe70Leu
ENST00000294304.12:c.208T>C MANE Select	ENSP00000294304.6:p.Phe70Leu
NM_001291902.1:c.-1558T>C	NP_001278831.1:n.-1558T>C
NM_001291902.2:c.-1558T>C	NP_001278831.1:n.-1558T>C
NM_002335.3:c.208T>C	NP_002326.2:p.Phe70Leu
ENST00000294304.11:c.208T>C	ENSP00000294304.6:p.Phe70Leu
ENST00000529993.5:c.208T>C	ENSP00000436652.1:p.Phe70Leu
XM_005273994.2:c.208T>C	XP_005274051.1:p.Phe70Leu
XM_011545029.1:c.235T>C	XP_011543331.1:p.Phe79Leu
XM_011545030.1:c.235T>C	XP_011543332.1:p.Phe79Leu
XM_011545031.1:c.235T>C	XP_011543333.1:p.Phe79Leu
XR_001747874.1:n.250T>C
XR_949925.1:n.250T>C
XR_949925.2:n.250T>C
XR_949926.1:n.250T>C
XR_949926.2:n.250T>C