Canonical Allele Identifier: CA381613781
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68433701A>T , CM000673.2:g.68433701A>T GRCh38
NC_000011.9:g.68201169A>T , CM000673.1:g.68201169A>T GRCh37
NC_000011.8:g.67957745A>T NCBI36
NG_015835.1:g.126062A>T
NG_015835.2:g.126062A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.3863A>T MANE Select ENSP00000294304.6:p.Asp1288Val
ENST00000294304.11:c.3863A>T ENSP00000294304.6:p.Asp1288Val
ENST00000529993.5:c.*2469A>T ENSP00000436652.1:n.*2469A>T
NM_001291902.1:c.2120A>T NP_001278831.1:p.Asp707Val
NM_002335.3:c.3863A>T NP_002326.2:p.Asp1288Val
XM_005273994.2:c.3863A>T XP_005274051.1:p.Asp1288Val
XM_011545029.1:c.3890A>T XP_011543331.1:p.Asp1297Val
XM_011545030.1:c.3890A>T XP_011543332.1:p.Asp1297Val
XM_011545031.1:c.3890A>T XP_011543333.1:p.Asp1297Val
XR_949925.1:n.3905A>T
XR_949926.1:n.3905A>T
XM_017017735.1:c.2120A>T XP_016873224.1:p.Asp707Val
XM_017017736.1:c.1403A>T XP_016873225.1:p.Asp468Val
XR_949925.2:n.3905A>T
XR_949926.2:n.3905A>T
NM_002335.4:c.3863A>T MANE Select NP_002326.2:p.Asp1288Val
NM_001291902.2:c.2120A>T NP_001278831.1:p.Asp707Val