Canonical Allele Identifier: CA13744400

Gene: LRP6 BCL2L14

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12125534A>T , CM000674.2:g.12125534A>T	GRCh38
NC_000012.11:g.12278468A>T , CM000674.1:g.12278468A>T	GRCh37
NC_000012.10:g.12169735A>T	NCBI36
NG_016168.1:g.146344T>A
NG_016168.2:g.146344T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002336.3:c.4313-102T>A (LRP6) MANE Select	NP_002327.2:n.4313-102T>A
ENST00000261349.9:c.4313-102T>A (LRP6) MANE Select	ENSP00000261349.4:n.4313-102T>A
NM_002336.2:c.4313-102T>A (LRP6)	NP_002327.2:n.4313-102T>A
ENST00000261349.8:c.4313-102T>A (LRP6)	ENSP00000261349.4:n.4313-102T>A
ENST00000298566.2:c.711+10207A>T (BCL2L14)	ENSP00000298566.1:n.711+10207A>T
ENST00000538239.5:c.3907-102T>A (LRP6)
ENST00000540415.1:n.403-102T>A (LRP6)
ENST00000540527.5:c.122-872T>A (LRP6)	ENSP00000443239.1:n.122-872T>A
ENST00000543091.1:c.4178-102T>A (LRP6)	ENSP00000442472.1:n.4178-102T>A
XM_006719078.2:c.4313-102T>A (LRP6)	XP_006719141.1:n.4313-102T>A
XM_006719078.4:c.4313-102T>A (LRP6)	XP_006719141.1:n.4313-102T>A
XM_011520671.1:c.3860-102T>A (LRP6)	XP_011518973.1:n.3860-102T>A
XM_011520671.3:c.3860-102T>A (LRP6)	XP_011518973.1:n.3860-102T>A
XR_002957325.1:n.4446-102T>A (LRP6)
XR_429034.1:n.4446-102T>A (LRP6)
XR_429035.1:n.4446-102T>A (LRP6)
XR_429035.3:n.4446-102T>A (LRP6)