Canonical Allele Identifier: CA5969213
Community Standard Title: NM_002334.4(LRP4):c.4890C>T (p.Ala1630=)
Gene: LRP4 HGNC NCBI
LRP4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46868661G>A , CM000673.2:g.46868661G>A GRCh38
NC_000011.9:g.46890212G>A , CM000673.1:g.46890212G>A GRCh37
NC_000011.8:g.46846788G>A NCBI36
NG_021394.1:g.54962C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.4890C>T (LRP4) MANE Select NP_002325.2:p.Ala1630=
ENST00000378623.6:c.4890C>T (LRP4) MANE Select ENSP00000367888.1:p.Ala1630=
NM_002334.3:c.4890C>T (LRP4) NP_002325.2:p.Ala1630=
NR_038909.1:n.198-4413G>A (LRP4-AS1)
ENST00000378623.5:c.4890C>T (LRP4) ENSP00000367888.1:p.Ala1630=
XM_011520102.1:c.5103C>T (LRP4) XP_011518404.1:p.Ala1701=
XM_011520103.1:c.4086C>T (LRP4) XP_011518405.1:p.Ala1362=
XM_011520103.2:c.4086C>T (LRP4) XP_011518405.1:p.Ala1362=
XM_011520104.1:c.2655C>T (LRP4) XP_011518406.1:p.Ala885=
XM_011520104.2:c.2655C>T (LRP4) XP_011518406.1:p.Ala885=
XM_017017734.1:c.4890C>T (LRP4) XP_016873223.1:p.Ala1630=