Canonical Allele Identifier: CA1969122432
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46875806C= , CM000673.2:g.46875806C= GRCh38
NC_000011.9:g.46897357C= , CM000673.1:g.46897357C= GRCh37
NC_000011.8:g.46853933C= NCBI36
NG_021394.1:g.47817G=

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3697G= MANE Select NP_002325.2:p.Glu1233=
ENST00000378623.6:c.3697G= MANE Select ENSP00000367888.1:p.Glu1233=
NM_002334.3:c.3697G= NP_002325.2:p.Glu1233=
ENST00000378623.5:c.3697G= ENSP00000367888.1:p.Glu1233=
XM_011520102.1:c.3910G= XP_011518404.1:p.Glu1304=
XM_011520103.1:c.2893G= XP_011518405.1:p.Glu965=
XM_011520103.2:c.2893G= XP_011518405.1:p.Glu965=
XM_011520104.1:c.1462G= XP_011518406.1:p.Glu488=
XM_011520104.2:c.1462G= XP_011518406.1:p.Glu488=
XM_017017734.1:c.3697G= XP_016873223.1:p.Glu1233=