Canonical Allele Identifier: CA381616774

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68213910A>T (hg19) ; chr11:g.68446442A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68446442A>T , CM000673.2:g.68446442A>T	GRCh38
NC_000011.9:g.68213910A>T , CM000673.1:g.68213910A>T	GRCh37
NC_000011.8:g.67970486A>T	NCBI36
NG_015835.1:g.138803A>T
NG_015835.2:g.138803A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.4495A>T MANE Select	ENSP00000294304.6:p.Asn1499Tyr
ENST00000294304.11:c.4495A>T	ENSP00000294304.6:p.Asn1499Tyr
ENST00000529702.1:c.165A>T
ENST00000529993.5:c.*3101A>T	ENSP00000436652.1:n.*3101A>T
NM_001291902.1:c.2752A>T	NP_001278831.1:p.Asn918Tyr
NM_002335.3:c.4495A>T	NP_002326.2:p.Asn1499Tyr
XM_005273994.2:c.4609A>T	XP_005274051.1:p.Asn1537Tyr
XM_011545029.1:c.4636A>T	XP_011543331.1:p.Asn1546Tyr
XM_011545030.1:c.4522A>T	XP_011543332.1:p.Asn1508Tyr
XM_011545031.1:c.4652A>T	XP_011543333.1:p.Glu1551Val
XR_949925.1:n.4651A>T
XR_949926.1:n.4667A>T
XM_017017735.1:c.2866A>T	XP_016873224.1:p.Asn956Tyr
XM_017017736.1:c.2149A>T	XP_016873225.1:p.Asn717Tyr
XR_949925.2:n.4651A>T
XR_949926.2:n.4667A>T
NM_002335.4:c.4495A>T MANE Select	NP_002326.2:p.Asn1499Tyr
NM_001291902.2:c.2752A>T	NP_001278831.1:p.Asn918Tyr