Canonical Allele Identifier: CA16042789
Gene: LRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46875651_46875652delinsAA , CM000673.2:g.46875651_46875652delinsAA GRCh38
NC_000011.9:g.46897202_46897203delinsAA , CM000673.1:g.46897202_46897203delinsAA GRCh37
NC_000011.8:g.46853778_46853779delinsAA NCBI36
NG_021394.1:g.47971_47972delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378623.6:c.3729_3730delinsTT MANE Select ENSP00000367888.1:p.Asn1244Tyr
ENST00000378623.5:c.3729_3730delinsTT ENSP00000367888.1:p.Asn1244Tyr
NM_002334.3:c.3729_3730delinsTT NP_002325.2:p.Asn1244Tyr
XM_011520102.1:c.3942_3943delinsTT XP_011518404.1:p.Asn1315Tyr
XM_011520103.1:c.2925_2926delinsTT XP_011518405.1:p.Asn976Tyr
XM_011520104.1:c.1494_1495delinsTT XP_011518406.1:p.Asn499Tyr
XM_011520103.2:c.2925_2926delinsTT XP_011518405.1:p.Asn976Tyr
XM_011520104.2:c.1494_1495delinsTT XP_011518406.1:p.Asn499Tyr
XM_017017734.1:c.3729_3730delinsTT XP_016873223.1:p.Asn1244Tyr
NM_002334.4:c.3729_3730delinsTT MANE Select NP_002325.2:p.Asn1244Tyr