Canonical Allele Identifier: CA478661517
Gene: LRP6 HGNC NCBI
BCL2L14 HGNC NCBI

Linked Data

dbSNP Id: rs1385269132
MyVariant Identifiers: chr12:g.12334177T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12181243T>A , CM000674.2:g.12181243T>A GRCh38
NC_000012.11:g.12334177T>A , CM000674.1:g.12334177T>A GRCh37
NC_000012.10:g.12225444T>A NCBI36
NG_016168.1:g.90635A>T
NG_016168.2:g.90635A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261349.9:c.1173A>T (LRP6) MANE Select ENSP00000261349.4:p.Gly391=
ENST00000261349.8:c.1173A>T (LRP6) ENSP00000261349.4:p.Gly391=
ENST00000298566.2:c.*25-6062T>A (BCL2L14) ENSP00000298566.1:n.*25-6062T>A
ENST00000538239.5:c.767A>T (LRP6)
ENST00000543091.1:c.1173A>T (LRP6) ENSP00000442472.1:p.Gly391=
NM_002336.2:c.1173A>T (LRP6) NP_002327.2:p.Gly391=
XM_006719078.2:c.1173A>T (LRP6) XP_006719141.1:p.Gly391=
XM_011520671.1:c.720A>T (LRP6) XP_011518973.1:p.Gly240=
XR_429034.1:n.1306A>T (LRP6)
XR_429035.1:n.1306A>T (LRP6)
XM_006719078.4:c.1173A>T (LRP6) XP_006719141.1:p.Gly391=
XM_011520671.3:c.720A>T (LRP6) XP_011518973.1:p.Gly240=
XR_002957325.1:n.1306A>T (LRP6)
XR_429035.3:n.1306A>T (LRP6)
NM_002336.3:c.1173A>T (LRP6) MANE Select NP_002327.2:p.Gly391=