Canonical Allele Identifier: CA1969122601
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46875946C= , CM000673.2:g.46875946C= GRCh38
NC_000011.9:g.46897497C= , CM000673.1:g.46897497C= GRCh37
NC_000011.8:g.46854073C= NCBI36
NG_021394.1:g.47677G=

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3557G= MANE Select NP_002325.2:p.Trp1186=
ENST00000378623.6:c.3557G= MANE Select ENSP00000367888.1:p.Trp1186=
NM_002334.3:c.3557G= NP_002325.2:p.Trp1186=
ENST00000378623.5:c.3557G= ENSP00000367888.1:p.Trp1186=
XM_011520102.1:c.3770G= XP_011518404.1:p.Trp1257=
XM_011520103.1:c.2753G= XP_011518405.1:p.Trp918=
XM_011520103.2:c.2753G= XP_011518405.1:p.Trp918=
XM_011520104.1:c.1322G= XP_011518406.1:p.Trp441=
XM_011520104.2:c.1322G= XP_011518406.1:p.Trp441=
XM_017017734.1:c.3557G= XP_016873223.1:p.Trp1186=