Canonical Allele Identifier: CA381610105

Gene: LRP5

Linked Data

• dbSNP Id: rs770308939
• MyVariant Identifiers: chr11:g.68115339A>C (hg19) ; chr11:g.68347871A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68347871A>C , CM000673.2:g.68347871A>C	GRCh38
NC_000011.9:g.68115339A>C , CM000673.1:g.68115339A>C	GRCh37
NC_000011.8:g.67871915A>C	NCBI36
NG_015835.1:g.40232A>C
NG_015835.2:g.40232A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.116A>C MANE Select	ENSP00000294304.6:p.Asn39Thr
ENST00000294304.11:c.116A>C	ENSP00000294304.6:p.Asn39Thr
ENST00000529993.5:c.116A>C	ENSP00000436652.1:p.Asn39Thr
NM_001291902.1:c.-1650A>C	NP_001278831.1:n.-1650A>C
NM_002335.3:c.116A>C	NP_002326.2:p.Asn39Thr
XM_005273994.2:c.116A>C	XP_005274051.1:p.Asn39Thr
XM_011545029.1:c.143A>C	XP_011543331.1:p.Asn48Thr
XM_011545030.1:c.143A>C	XP_011543332.1:p.Asn48Thr
XM_011545031.1:c.143A>C	XP_011543333.1:p.Asn48Thr
XR_949925.1:n.158A>C
XR_949926.1:n.158A>C
XR_001747874.1:n.158A>C
XR_949925.2:n.158A>C
XR_949926.2:n.158A>C
NM_002335.4:c.116A>C MANE Select	NP_002326.2:p.Asn39Thr
NM_001291902.2:c.-1650A>C	NP_001278831.1:n.-1650A>C