Canonical Allele Identifier: CA358758
Gene: LRP6 HGNC NCBI
BCL2L14 HGNC NCBI

Linked Data

ClinVar Variation Id: 225147
ClinVar RCV Id: RCV000210778
dbSNP Id: rs869320635

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12121377del , CM000674.2:g.12121377del GRCh38
NC_000012.11:g.12274311del , CM000674.1:g.12274311del GRCh37
NC_000012.10:g.12165578del NCBI36
NG_016168.1:g.150503del
NG_016168.2:g.150503del

Transcript Alleles

HGVS Amino-acid change
ENST00000261349.9:c.4593del (LRP6) MANE Select ENSP00000261349.4:p.Cys1532AlafsTer16
ENST00000261349.8:c.4593del (LRP6) ENSP00000261349.4:p.Cys1532AlafsTer16
ENST00000298566.2:c.711+6050del (BCL2L14) ENSP00000298566.1:n.711+6050del
ENST00000538239.5:c.4187del (LRP6)
ENST00000540527.5:c.265del (LRP6) ENSP00000443239.1:n.265del
ENST00000543091.1:c.4458del (LRP6) ENSP00000442472.1:p.Cys1487AlafsTer16
NM_002336.2:c.4593del (LRP6) NP_002327.2:p.Cys1532AlafsTer16
XM_006719078.2:c.4593del (LRP6) XP_006719141.1:p.Cys1532AlafsTer16
XM_011520671.1:c.4140del (LRP6) XP_011518973.1:p.Cys1381AlafsTer16
XR_429034.1:n.4726del (LRP6)
XR_429035.1:n.4726del (LRP6)
XM_006719078.4:c.4593del (LRP6) XP_006719141.1:p.Cys1532AlafsTer16
XM_011520671.3:c.4140del (LRP6) XP_011518973.1:p.Cys1381AlafsTer16
XR_002957325.1:n.4726del (LRP6)
XR_429035.3:n.4726del (LRP6)
NM_002336.3:c.4593del (LRP6) MANE Select NP_002327.2:p.Cys1532AlafsTer16