Canonical Allele Identifier: CA5969061
Community Standard Title: NM_002334.4(LRP4):c.5346C>G (p.Pro1782=)
Gene: LRP4 HGNC NCBI
LRP4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46862645G>C , CM000673.2:g.46862645G>C GRCh38
NC_000011.9:g.46884196G>C , CM000673.1:g.46884196G>C GRCh37
NC_000011.8:g.46840772G>C NCBI36
NG_021394.1:g.60978C>G

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.5346C>G (LRP4) MANE Select NP_002325.2:p.Pro1782=
ENST00000378623.6:c.5346C>G (LRP4) MANE Select ENSP00000367888.1:p.Pro1782=
NM_002334.3:c.5346C>G (LRP4) NP_002325.2:p.Pro1782=
NR_038909.1:n.198-10429G>C (LRP4-AS1)
ENST00000378623.5:c.5346C>G (LRP4) ENSP00000367888.1:p.Pro1782=
ENST00000529604.1:n.289C>G (LRP4)
XM_011520102.1:c.5559C>G (LRP4) XP_011518404.1:p.Pro1853=
XM_011520103.1:c.4542C>G (LRP4) XP_011518405.1:p.Pro1514=
XM_011520103.2:c.4542C>G (LRP4) XP_011518405.1:p.Pro1514=
XM_011520104.1:c.3111C>G (LRP4) XP_011518406.1:p.Pro1037=
XM_011520104.2:c.3111C>G (LRP4) XP_011518406.1:p.Pro1037=
XM_017017734.1:c.5346C>G (LRP4) XP_016873223.1:p.Pro1782=