Canonical Allele Identifier: CA2016768327

Gene: LRP6 BCL2L14

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12131984C= , CM000674.2:g.12131984C=	GRCh38
NC_000012.11:g.12284918C= , CM000674.1:g.12284918C=	GRCh37
NC_000012.10:g.12176185C=	NCBI36
NG_016168.1:g.139894G=
NG_016168.2:g.139894G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261349.9:c.3807G= (LRP6) MANE Select	ENSP00000261349.4:p.Arg1269=
ENST00000261349.8:c.3807G= (LRP6)	ENSP00000261349.4:p.Arg1269=
ENST00000298566.2:c.712-6852C= (BCL2L14)	ENSP00000298566.1:n.712-6852C=
ENST00000538239.5:c.3401G= (LRP6)
ENST00000540415.1:n.128G= (LRP6)
ENST00000543091.1:c.3734-62G= (LRP6)	ENSP00000442472.1:n.3734-62G=
NM_002336.2:c.3807G= (LRP6)	NP_002327.2:p.Arg1269=
XM_006719078.2:c.3807G= (LRP6)	XP_006719141.1:p.Arg1269=
XM_011520671.1:c.3354G= (LRP6)	XP_011518973.1:p.Arg1118=
XR_429034.1:n.3940G= (LRP6)
XR_429035.1:n.3940G= (LRP6)
XM_006719078.4:c.3807G= (LRP6)	XP_006719141.1:p.Arg1269=
XM_011520671.3:c.3354G= (LRP6)	XP_011518973.1:p.Arg1118=
XR_002957325.1:n.3940G= (LRP6)
XR_429035.3:n.3940G= (LRP6)
NM_002336.3:c.3807G= (LRP6) MANE Select	NP_002327.2:p.Arg1269=