Canonical Allele Identifier: CA475462505

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68216295A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68448827A>C , CM000673.2:g.68448827A>C	GRCh38
NC_000011.9:g.68216295A>C , CM000673.1:g.68216295A>C	GRCh37
NC_000011.8:g.67972871A>C	NCBI36
NG_015835.1:g.141188A>C
NG_015835.2:g.141188A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4605A>C MANE Select	ENSP00000294304.6:p.Gly1535=
ENST00000294304.11:c.4605A>C	ENSP00000294304.6:p.Gly1535=
ENST00000529481.1:n.196A>C
ENST00000529702.1:c.275A>C
ENST00000529993.5:c.*3211A>C	ENSP00000436652.1:n.*3211A>C
NM_001291902.1:c.2862A>C	NP_001278831.1:p.Gly954=
NM_002335.3:c.4605A>C	NP_002326.2:p.Gly1535=
XM_005273994.2:c.4719A>C	XP_005274051.1:p.Gly1573=
XM_011545029.1:c.4746A>C	XP_011543331.1:p.Gly1582=
XM_011545030.1:c.4632A>C	XP_011543332.1:p.Gly1544=
XM_011545031.1:c.4762A>C	XP_011543333.1:p.Asn1588His
XR_949925.1:n.4992A>C
XR_949926.1:n.5008A>C
XM_017017735.1:c.2976A>C	XP_016873224.1:p.Gly992=
XM_017017736.1:c.2259A>C	XP_016873225.1:p.Gly753=
XR_949925.2:n.4992A>C
XR_949926.2:n.5008A>C
NM_002335.4:c.4605A>C MANE Select	NP_002326.2:p.Gly1535=
NM_001291902.2:c.2862A>C	NP_001278831.1:p.Gly954=