Canonical Allele Identifier: CA2739271870
Gene: LRP6 HGNC NCBI
BCL2L14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2864096
ClinVar RCV Id: RCV003702597

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12181248_12181254del , CM000674.2:g.12181248_12181254del GRCh38
NC_000012.11:g.12334182_12334188del , CM000674.1:g.12334182_12334188del GRCh37
NC_000012.10:g.12225449_12225455del NCBI36
NG_016168.1:g.90624_90630del
NG_016168.2:g.90624_90630del

Transcript Alleles

HGVS Amino-acid change
ENST00000261349.9:c.1162_1168del (LRP6) MANE Select ENSP00000261349.4:p.Phe388MetfsTer?
ENST00000261349.8:c.1162_1168del (LRP6) ENSP00000261349.4:p.Phe388MetfsTer?
ENST00000298566.2:c.*25-6057_*25-6051del (BCL2L14) ENSP00000298566.1:n.*25-6057_*25-6051del
ENST00000538239.5:c.756_762del (LRP6)
ENST00000543091.1:c.1162_1168del (LRP6) ENSP00000442472.1:p.Phe388MetfsTer?
NM_002336.2:c.1162_1168del (LRP6) NP_002327.2:p.Phe388MetfsTer?
XM_006719078.2:c.1162_1168del (LRP6) XP_006719141.1:p.Phe388MetfsTer?
XM_011520671.1:c.709_715del (LRP6) XP_011518973.1:p.Phe237MetfsTer?
XR_429034.1:n.1295_1301del (LRP6)
XR_429035.1:n.1295_1301del (LRP6)
XM_006719078.4:c.1162_1168del (LRP6) XP_006719141.1:p.Phe388MetfsTer?
XM_011520671.3:c.709_715del (LRP6) XP_011518973.1:p.Phe237MetfsTer?
XR_002957325.1:n.1295_1301del (LRP6)
XR_429035.3:n.1295_1301del (LRP6)
NM_002336.3:c.1162_1168del (LRP6) MANE Select NP_002327.2:p.Phe388MetfsTer?