Canonical Allele Identifier: CA1969121955
Community Standard Title: NM_002334.4(LRP4):c.3925+99C=
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46875357G= , CM000673.2:g.46875357G= GRCh38
NC_000011.9:g.46896908G= , CM000673.1:g.46896908G= GRCh37
NC_000011.8:g.46853484G= NCBI36
NG_021394.1:g.48266C=

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3925+99C= MANE Select NP_002325.2:n.3925+99C=
ENST00000378623.6:c.3925+99C= MANE Select ENSP00000367888.1:n.3925+99C=
NM_002334.3:c.3925+99C= NP_002325.2:n.3925+99C=
ENST00000378623.5:c.3925+99C= ENSP00000367888.1:n.3925+99C=
XM_011520102.1:c.4138+99C= XP_011518404.1:n.4138+99C=
XM_011520103.1:c.3121+99C= XP_011518405.1:n.3121+99C=
XM_011520103.2:c.3121+99C= XP_011518405.1:n.3121+99C=
XM_011520104.1:c.1690+99C= XP_011518406.1:n.1690+99C=
XM_011520104.2:c.1690+99C= XP_011518406.1:n.1690+99C=
XM_017017734.1:c.3925+99C= XP_016873223.1:n.3925+99C=