Canonical Allele Identifier: CA1980629325

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68347780T= , CM000673.2:g.68347780T=	GRCh38
NC_000011.9:g.68115248T= , CM000673.1:g.68115248T=	GRCh37
NC_000011.8:g.67871824T=	NCBI36
NG_015835.1:g.40141T=
NG_015835.2:g.40141T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.92-67T= MANE Select	ENSP00000294304.6:n.92-67T=
ENST00000294304.11:c.92-67T=	ENSP00000294304.6:n.92-67T=
ENST00000529993.5:c.92-67T=	ENSP00000436652.1:n.92-67T=
NM_001291902.1:c.-1674-67T=	NP_001278831.1:n.-1674-67T=
NM_002335.3:c.92-67T=	NP_002326.2:n.92-67T=
XM_005273994.2:c.92-67T=	XP_005274051.1:n.92-67T=
XM_011545029.1:c.119-67T=	XP_011543331.1:n.119-67T=
XM_011545030.1:c.119-67T=	XP_011543332.1:n.119-67T=
XM_011545031.1:c.119-67T=	XP_011543333.1:n.119-67T=
XR_949925.1:n.134-67T=
XR_949926.1:n.134-67T=
XR_001747874.1:n.134-67T=
XR_949925.2:n.134-67T=
XR_949926.2:n.134-67T=
NM_002335.4:c.92-67T= MANE Select	NP_002326.2:n.92-67T=
NM_001291902.2:c.-1674-67T=	NP_001278831.1:n.-1674-67T=