Canonical Allele Identifier: CA478843849

Gene: LRP6 BCL2L14

Linked Data

• dbSNP Id: rs1591868438
• MyVariant Identifiers: chr12:g.12284927C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12131993C>T , CM000674.2:g.12131993C>T	GRCh38
NC_000012.11:g.12284927C>T , CM000674.1:g.12284927C>T	GRCh37
NC_000012.10:g.12176194C>T	NCBI36
NG_016168.1:g.139885G>A
NG_016168.2:g.139885G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261349.9:c.3798G>A (LRP6) MANE Select	ENSP00000261349.4:p.Val1266=
ENST00000261349.8:c.3798G>A (LRP6)	ENSP00000261349.4:p.Val1266=
ENST00000298566.2:c.712-6843C>T (BCL2L14)	ENSP00000298566.1:n.712-6843C>T
ENST00000538239.5:c.3392G>A (LRP6)
ENST00000540415.1:n.119G>A (LRP6)
ENST00000543091.1:c.3734-71G>A (LRP6)	ENSP00000442472.1:n.3734-71G>A
NM_002336.2:c.3798G>A (LRP6)	NP_002327.2:p.Val1266=
XM_006719078.2:c.3798G>A (LRP6)	XP_006719141.1:p.Val1266=
XM_011520671.1:c.3345G>A (LRP6)	XP_011518973.1:p.Val1115=
XR_429034.1:n.3931G>A (LRP6)
XR_429035.1:n.3931G>A (LRP6)
XM_006719078.4:c.3798G>A (LRP6)	XP_006719141.1:p.Val1266=
XM_011520671.3:c.3345G>A (LRP6)	XP_011518973.1:p.Val1115=
XR_002957325.1:n.3931G>A (LRP6)
XR_429035.3:n.3931G>A (LRP6)
NM_002336.3:c.3798G>A (LRP6) MANE Select	NP_002327.2:p.Val1266=