Canonical Allele Identifier: CA383946323
Gene: LRP6 HGNC NCBI
BCL2L14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12164296A>T , CM000674.2:g.12164296A>T GRCh38
NC_000012.11:g.12317230A>T , CM000674.1:g.12317230A>T GRCh37
NC_000012.10:g.12208497A>T NCBI36
NG_016168.1:g.107582T>A
NG_016168.2:g.107582T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261349.9:c.2029T>A (LRP6) MANE Select ENSP00000261349.4:p.Tyr677Asn
ENST00000261349.8:c.2029T>A (LRP6) ENSP00000261349.4:p.Tyr677Asn
ENST00000298566.2:c.*25-23009A>T (BCL2L14) ENSP00000298566.1:n.*25-23009A>T
ENST00000538239.5:c.1623T>A (LRP6)
ENST00000543091.1:c.2029T>A (LRP6) ENSP00000442472.1:p.Tyr677Asn
NM_002336.2:c.2029T>A (LRP6) NP_002327.2:p.Tyr677Asn
XM_006719078.2:c.2029T>A (LRP6) XP_006719141.1:p.Tyr677Asn
XM_011520671.1:c.1576T>A (LRP6) XP_011518973.1:p.Tyr526Asn
XR_429034.1:n.2162T>A (LRP6)
XR_429035.1:n.2162T>A (LRP6)
XM_006719078.4:c.2029T>A (LRP6) XP_006719141.1:p.Tyr677Asn
XM_011520671.3:c.1576T>A (LRP6) XP_011518973.1:p.Tyr526Asn
XR_002957325.1:n.2162T>A (LRP6)
XR_429035.3:n.2162T>A (LRP6)
NM_002336.3:c.2029T>A (LRP6) MANE Select NP_002327.2:p.Tyr677Asn