Canonical Allele Identifier: CA1969123090
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46876494G= , CM000673.2:g.46876494G= GRCh38
NC_000011.9:g.46898045G= , CM000673.1:g.46898045G= GRCh37
NC_000011.8:g.46854621G= NCBI36
NG_021394.1:g.47129C=

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3508C= MANE Select NP_002325.2:p.Arg1170=
ENST00000378623.6:c.3508C= MANE Select ENSP00000367888.1:p.Arg1170=
NM_002334.3:c.3508C= NP_002325.2:p.Arg1170=
ENST00000378623.5:c.3508C= ENSP00000367888.1:p.Arg1170=
XM_011520102.1:c.3721C= XP_011518404.1:p.Arg1241=
XM_011520103.1:c.2704C= XP_011518405.1:p.Arg902=
XM_011520103.2:c.2704C= XP_011518405.1:p.Arg902=
XM_011520104.1:c.1273C= XP_011518406.1:p.Arg425=
XM_011520104.2:c.1273C= XP_011518406.1:p.Arg425=
XM_017017734.1:c.3508C= XP_016873223.1:p.Arg1170=