Canonical Allele Identifier: CA1980666620
Gene: LRP5 HGNC NCBI

Linked Data

dbSNP Id: rs1565126792

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68448636G>T , CM000673.2:g.68448636G>T GRCh38
NC_000011.9:g.68216104G>T , CM000673.1:g.68216104G>T GRCh37
NC_000011.8:g.67972680G>T NCBI36
NG_015835.1:g.140997G>T
NG_015835.2:g.140997G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.4587-173G>T MANE Select ENSP00000294304.6:n.4587-173G>T
ENST00000294304.11:c.4587-173G>T ENSP00000294304.6:n.4587-173G>T
ENST00000529481.1:n.178-173G>T
ENST00000529702.1:c.257-173G>T
ENST00000529993.5:c.*3193-173G>T ENSP00000436652.1:n.*3193-173G>T
NM_001291902.1:c.2844-173G>T NP_001278831.1:n.2844-173G>T
NM_002335.3:c.4587-173G>T NP_002326.2:n.4587-173G>T
XM_005273994.2:c.4701-173G>T XP_005274051.1:n.4701-173G>T
XM_011545029.1:c.4728-173G>T XP_011543331.1:n.4728-173G>T
XM_011545030.1:c.4614-173G>T XP_011543332.1:n.4614-173G>T
XM_011545031.1:c.4744-173G>T XP_011543333.1:n.4744-173G>T
XR_949925.1:n.4974-173G>T
XR_949926.1:n.4990-173G>T
XM_017017735.1:c.2958-173G>T XP_016873224.1:n.2958-173G>T
XM_017017736.1:c.2241-173G>T XP_016873225.1:n.2241-173G>T
XR_949925.2:n.4974-173G>T
XR_949926.2:n.4990-173G>T
NM_002335.4:c.4587-173G>T MANE Select NP_002326.2:n.4587-173G>T
NM_001291902.2:c.2844-173G>T NP_001278831.1:n.2844-173G>T