Canonical Allele Identifier: CA2614713107
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68406412_68406413insA , CM000673.2:g.68406412_68406413insA GRCh38
NC_000011.9:g.68173880_68173881insA , CM000673.1:g.68173880_68173881insA GRCh37
NC_000011.8:g.67930456_67930457insA NCBI36
NG_015835.1:g.98773_98774insA
NG_015835.2:g.98773_98774insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1802-112_1802-111insA MANE Select ENSP00000294304.6:n.1802-112_1802-111insA
ENST00000294304.11:c.1802-112_1802-111insA ENSP00000294304.6:n.1802-112_1802-111insA
ENST00000528890.1:n.441-112_441-111insA
ENST00000529993.5:c.*408-112_*408-111insA ENSP00000436652.1:n.*408-112_*408-111insA
NM_001291902.1:c.59-112_59-111insA NP_001278831.1:n.59-112_59-111insA
NM_002335.3:c.1802-112_1802-111insA NP_002326.2:n.1802-112_1802-111insA
XM_005273994.2:c.1802-112_1802-111insA XP_005274051.1:n.1802-112_1802-111insA
XM_011545029.1:c.1829-112_1829-111insA XP_011543331.1:n.1829-112_1829-111insA
XM_011545030.1:c.1829-112_1829-111insA XP_011543332.1:n.1829-112_1829-111insA
XM_011545031.1:c.1829-112_1829-111insA XP_011543333.1:n.1829-112_1829-111insA
XR_949925.1:n.1844-112_1844-111insA
XR_949926.1:n.1844-112_1844-111insA
XM_017017735.1:c.59-112_59-111insA XP_016873224.1:n.59-112_59-111insA
XR_001747874.1:n.1844-112_1844-111insA
XR_949925.2:n.1844-112_1844-111insA
XR_949926.2:n.1844-112_1844-111insA
NM_002335.4:c.1802-112_1802-111insA MANE Select NP_002326.2:n.1802-112_1802-111insA
NM_001291902.2:c.59-112_59-111insA NP_001278831.1:n.59-112_59-111insA