Canonical Allele Identifier: CA475460121

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68125148G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68357680G>C , CM000673.2:g.68357680G>C	GRCh38
NC_000011.9:g.68125148G>C , CM000673.1:g.68125148G>C	GRCh37
NC_000011.8:g.67881724G>C	NCBI36
NG_015835.1:g.50041G>C
NG_015835.2:g.50041G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.519G>C MANE Select	ENSP00000294304.6:p.Thr173=
ENST00000294304.11:c.519G>C	ENSP00000294304.6:p.Thr173=
ENST00000529993.5:c.519G>C	ENSP00000436652.1:p.Thr173=
NM_001291902.1:c.-1247G>C	NP_001278831.1:n.-1247G>C
NM_002335.3:c.519G>C	NP_002326.2:p.Thr173=
XM_005273994.2:c.519G>C	XP_005274051.1:p.Thr173=
XM_011545029.1:c.546G>C	XP_011543331.1:p.Thr182=
XM_011545030.1:c.546G>C	XP_011543332.1:p.Thr182=
XM_011545031.1:c.546G>C	XP_011543333.1:p.Thr182=
XR_949925.1:n.561G>C
XR_949926.1:n.561G>C
XR_001747874.1:n.561G>C
XR_949925.2:n.561G>C
XR_949926.2:n.561G>C
NM_002335.4:c.519G>C MANE Select	NP_002326.2:p.Thr173=
NM_001291902.2:c.-1247G>C	NP_001278831.1:n.-1247G>C