Canonical Allele Identifier: CA1980652015

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68403791T= , CM000673.2:g.68403791T=	GRCh38
NC_000011.9:g.68171259T= , CM000673.1:g.68171259T=	GRCh37
NC_000011.8:g.67927835T=	NCBI36
NG_015835.1:g.96152T=
NG_015835.2:g.96152T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1801+92T= MANE Select	ENSP00000294304.6:n.1801+92T=
ENST00000294304.11:c.1801+92T=	ENSP00000294304.6:n.1801+92T=
ENST00000529993.5:c.*213+92T=	ENSP00000436652.1:n.*213+92T=
NM_001291902.1:c.-137+92T=	NP_001278831.1:n.-137+92T=
NM_002335.3:c.1801+92T=	NP_002326.2:n.1801+92T=
XM_005273994.2:c.1801+92T=	XP_005274051.1:n.1801+92T=
XM_011545029.1:c.1828+92T=	XP_011543331.1:n.1828+92T=
XM_011545030.1:c.1828+92T=	XP_011543332.1:n.1828+92T=
XM_011545031.1:c.1828+92T=	XP_011543333.1:n.1828+92T=
XR_949925.1:n.1843+92T=
XR_949926.1:n.1843+92T=
XR_001747874.1:n.1843+92T=
XR_949925.2:n.1843+92T=
XR_949926.2:n.1843+92T=
NM_002335.4:c.1801+92T= MANE Select	NP_002326.2:n.1801+92T=
NM_001291902.2:c.-137+92T=	NP_001278831.1:n.-137+92T=