Canonical Allele Identifier: CA1969122154
Community Standard Title: NM_002334.4(LRP4):c.3830G= (p.Arg1277=)
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46875551C= , CM000673.2:g.46875551C= GRCh38
NC_000011.9:g.46897102C= , CM000673.1:g.46897102C= GRCh37
NC_000011.8:g.46853678C= NCBI36
NG_021394.1:g.48072G=

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3830G= MANE Select NP_002325.2:p.Arg1277=
ENST00000378623.6:c.3830G= MANE Select ENSP00000367888.1:p.Arg1277=
NM_002334.3:c.3830G= NP_002325.2:p.Arg1277=
ENST00000378623.5:c.3830G= ENSP00000367888.1:p.Arg1277=
XM_011520102.1:c.4043G= XP_011518404.1:p.Arg1348=
XM_011520103.1:c.3026G= XP_011518405.1:p.Arg1009=
XM_011520103.2:c.3026G= XP_011518405.1:p.Arg1009=
XM_011520104.1:c.1595G= XP_011518406.1:p.Arg532=
XM_011520104.2:c.1595G= XP_011518406.1:p.Arg532=
XM_017017734.1:c.3830G= XP_016873223.1:p.Arg1277=