Canonical Allele Identifier: CA380277552
Community Standard Title: NM_002334.4(LRP4):c.2866G>T (p.Glu956Ter)
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46879264C>A , CM000673.2:g.46879264C>A GRCh38
NC_000011.9:g.46900815C>A , CM000673.1:g.46900815C>A GRCh37
NC_000011.8:g.46857391C>A NCBI36
NG_021394.1:g.44359G>T

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.2866G>T MANE Select NP_002325.2:p.Glu956Ter
ENST00000378623.6:c.2866G>T MANE Select ENSP00000367888.1:p.Glu956Ter
NM_002334.3:c.2866G>T NP_002325.2:p.Glu956Ter
ENST00000378623.5:c.2866G>T ENSP00000367888.1:p.Glu956Ter
XM_011520102.1:c.3079G>T XP_011518404.1:p.Glu1027Ter
XM_011520103.1:c.2062G>T XP_011518405.1:p.Glu688Ter
XM_011520103.2:c.2062G>T XP_011518405.1:p.Glu688Ter
XM_011520104.1:c.631G>T XP_011518406.1:p.Glu211Ter
XM_011520104.2:c.631G>T XP_011518406.1:p.Glu211Ter
XM_017017734.1:c.2866G>T XP_016873223.1:p.Glu956Ter