Canonical Allele Identifier: CA1969122518
Community Standard Title: NM_002334.4(LRP4):c.3608C= (p.Ala1203=)
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46875895G= , CM000673.2:g.46875895G= GRCh38
NC_000011.9:g.46897446G= , CM000673.1:g.46897446G= GRCh37
NC_000011.8:g.46854022G= NCBI36
NG_021394.1:g.47728C=

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3608C= MANE Select NP_002325.2:p.Ala1203=
ENST00000378623.6:c.3608C= MANE Select ENSP00000367888.1:p.Ala1203=
NM_002334.3:c.3608C= NP_002325.2:p.Ala1203=
ENST00000378623.5:c.3608C= ENSP00000367888.1:p.Ala1203=
XM_011520102.1:c.3821C= XP_011518404.1:p.Ala1274=
XM_011520103.1:c.2804C= XP_011518405.1:p.Ala935=
XM_011520103.2:c.2804C= XP_011518405.1:p.Ala935=
XM_011520104.1:c.1373C= XP_011518406.1:p.Ala458=
XM_011520104.2:c.1373C= XP_011518406.1:p.Ala458=
XM_017017734.1:c.3608C= XP_016873223.1:p.Ala1203=