Canonical Allele Identifier: CA5969488
Community Standard Title: NM_002334.4(LRP4):c.3765A>G (p.Pro1255=)
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46875616T>C , CM000673.2:g.46875616T>C GRCh38
NC_000011.9:g.46897167T>C , CM000673.1:g.46897167T>C GRCh37
NC_000011.8:g.46853743T>C NCBI36
NG_021394.1:g.48007A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002334.4:c.3765A>G MANE Select NP_002325.2:p.Pro1255=
ENST00000378623.6:c.3765A>G MANE Select ENSP00000367888.1:p.Pro1255=
NM_002334.3:c.3765A>G NP_002325.2:p.Pro1255=
ENST00000378623.5:c.3765A>G ENSP00000367888.1:p.Pro1255=
XM_011520102.1:c.3978A>G XP_011518404.1:p.Pro1326=
XM_011520103.1:c.2961A>G XP_011518405.1:p.Pro987=
XM_011520103.2:c.2961A>G XP_011518405.1:p.Pro987=
XM_011520104.1:c.1530A>G XP_011518406.1:p.Pro510=
XM_011520104.2:c.1530A>G XP_011518406.1:p.Pro510=
XM_017017734.1:c.3765A>G XP_016873223.1:p.Pro1255=