Canonical Allele Identifier: CA475462507

Gene: LRP5

Linked Data

• gnomAD v4: 11-68448827-A-T
• MyVariant Identifiers: chr11:g.68216295A>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4605A>T MANE Select	ENSP00000294304.6:p.Gly1535=
ENST00000294304.11:c.4605A>T	ENSP00000294304.6:p.Gly1535=
ENST00000529481.1:n.196A>T
ENST00000529702.1:c.275A>T
ENST00000529993.5:c.*3211A>T	ENSP00000436652.1:n.*3211A>T
NM_001291902.1:c.2862A>T	NP_001278831.1:p.Gly954=
NM_002335.3:c.4605A>T	NP_002326.2:p.Gly1535=
XM_005273994.2:c.4719A>T	XP_005274051.1:p.Gly1573=
XM_011545029.1:c.4746A>T	XP_011543331.1:p.Gly1582=
XM_011545030.1:c.4632A>T	XP_011543332.1:p.Gly1544=
XM_011545031.1:c.4762A>T	XP_011543333.1:p.Asn1588Tyr
XR_949925.1:n.4992A>T
XR_949926.1:n.5008A>T
XM_017017735.1:c.2976A>T	XP_016873224.1:p.Gly992=
XM_017017736.1:c.2259A>T	XP_016873225.1:p.Gly753=
XR_949925.2:n.4992A>T
XR_949926.2:n.5008A>T
NM_002335.4:c.4605A>T MANE Select	NP_002326.2:p.Gly1535=
NM_001291902.2:c.2862A>T	NP_001278831.1:p.Gly954=