Canonical Allele Identifier: CA2016768329

Gene: LRP6 BCL2L14

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12131986G= , CM000674.2:g.12131986G=	GRCh38
NC_000012.11:g.12284920G= , CM000674.1:g.12284920G=	GRCh37
NC_000012.10:g.12176187G=	NCBI36
NG_016168.1:g.139892C=
NG_016168.2:g.139892C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261349.9:c.3805C= (LRP6) MANE Select	ENSP00000261349.4:p.Arg1269=
ENST00000261349.8:c.3805C= (LRP6)	ENSP00000261349.4:p.Arg1269=
ENST00000298566.2:c.712-6850G= (BCL2L14)	ENSP00000298566.1:n.712-6850G=
ENST00000538239.5:c.3399C= (LRP6)
ENST00000540415.1:n.126C= (LRP6)
ENST00000543091.1:c.3734-64C= (LRP6)	ENSP00000442472.1:n.3734-64C=
NM_002336.2:c.3805C= (LRP6)	NP_002327.2:p.Arg1269=
XM_006719078.2:c.3805C= (LRP6)	XP_006719141.1:p.Arg1269=
XM_011520671.1:c.3352C= (LRP6)	XP_011518973.1:p.Arg1118=
XR_429034.1:n.3938C= (LRP6)
XR_429035.1:n.3938C= (LRP6)
XM_006719078.4:c.3805C= (LRP6)	XP_006719141.1:p.Arg1269=
XM_011520671.3:c.3352C= (LRP6)	XP_011518973.1:p.Arg1118=
XR_002957325.1:n.3938C= (LRP6)
XR_429035.3:n.3938C= (LRP6)
NM_002336.3:c.3805C= (LRP6) MANE Select	NP_002327.2:p.Arg1269=