Canonical Allele Identifier: CA381614048
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68433830A>G , CM000673.2:g.68433830A>G GRCh38
NC_000011.9:g.68201298A>G , CM000673.1:g.68201298A>G GRCh37
NC_000011.8:g.67957874A>G NCBI36
NG_015835.1:g.126191A>G
NG_015835.2:g.126191A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.3992A>G MANE Select ENSP00000294304.6:p.Asp1331Gly
ENST00000294304.11:c.3992A>G ENSP00000294304.6:p.Asp1331Gly
ENST00000529993.5:c.*2598A>G ENSP00000436652.1:n.*2598A>G
NM_001291902.1:c.2249A>G NP_001278831.1:p.Asp750Gly
NM_002335.3:c.3992A>G NP_002326.2:p.Asp1331Gly
XM_005273994.2:c.3992A>G XP_005274051.1:p.Asp1331Gly
XM_011545029.1:c.4019A>G XP_011543331.1:p.Asp1340Gly
XM_011545030.1:c.4019A>G XP_011543332.1:p.Asp1340Gly
XM_011545031.1:c.4019A>G XP_011543333.1:p.Asp1340Gly
XR_949925.1:n.4034A>G
XR_949926.1:n.4034A>G
XM_017017735.1:c.2249A>G XP_016873224.1:p.Asp750Gly
XM_017017736.1:c.1532A>G XP_016873225.1:p.Asp511Gly
XR_949925.2:n.4034A>G
XR_949926.2:n.4034A>G
NM_002335.4:c.3992A>G MANE Select NP_002326.2:p.Asp1331Gly
NM_001291902.2:c.2249A>G NP_001278831.1:p.Asp750Gly