Canonical Allele Identifier: CA2724554902
Gene: LRP5 HGNC NCBI

Linked Data

dbSNP Id: rs2153185775

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68448608A>G , CM000673.2:g.68448608A>G GRCh38
NC_000011.9:g.68216076A>G , CM000673.1:g.68216076A>G GRCh37
NC_000011.8:g.67972652A>G NCBI36
NG_015835.1:g.140969A>G
NG_015835.2:g.140969A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.4587-201A>G MANE Select ENSP00000294304.6:n.4587-201A>G
ENST00000294304.11:c.4587-201A>G ENSP00000294304.6:n.4587-201A>G
ENST00000529481.1:n.178-201A>G
ENST00000529702.1:c.257-201A>G
ENST00000529993.5:c.*3193-201A>G ENSP00000436652.1:n.*3193-201A>G
NM_001291902.1:c.2844-201A>G NP_001278831.1:n.2844-201A>G
NM_002335.3:c.4587-201A>G NP_002326.2:n.4587-201A>G
XM_005273994.2:c.4701-201A>G XP_005274051.1:n.4701-201A>G
XM_011545029.1:c.4728-201A>G XP_011543331.1:n.4728-201A>G
XM_011545030.1:c.4614-201A>G XP_011543332.1:n.4614-201A>G
XM_011545031.1:c.4744-201A>G XP_011543333.1:n.4744-201A>G
XR_949925.1:n.4974-201A>G
XR_949926.1:n.4990-201A>G
XM_017017735.1:c.2958-201A>G XP_016873224.1:n.2958-201A>G
XM_017017736.1:c.2241-201A>G XP_016873225.1:n.2241-201A>G
XR_949925.2:n.4974-201A>G
XR_949926.2:n.4990-201A>G
NM_002335.4:c.4587-201A>G MANE Select NP_002326.2:n.4587-201A>G
NM_001291902.2:c.2844-201A>G NP_001278831.1:n.2844-201A>G