Canonical Allele Identifier: CA1980657292

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68439918T= , CM000673.2:g.68439918T=	GRCh38
NC_000011.9:g.68207386T= , CM000673.1:g.68207386T=	GRCh37
NC_000011.8:g.67963962T=	NCBI36
NG_015835.1:g.132279T=
NG_015835.2:g.132279T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.4488+2T= MANE Select	ENSP00000294304.6:n.4488+2T=
ENST00000294304.11:c.4488+2T=	ENSP00000294304.6:n.4488+2T=
ENST00000529702.1:c.44+2T=
ENST00000529993.5:c.*3094+2T=	ENSP00000436652.1:n.*3094+2T=
ENST00000533695.1:n.232T=
NM_001291902.1:c.2745+2T=	NP_001278831.1:n.2745+2T=
NM_002335.3:c.4488+2T=	NP_002326.2:n.4488+2T=
XM_005273994.2:c.4488+2T=	XP_005274051.1:n.4488+2T=
XM_011545029.1:c.4515+2T=	XP_011543331.1:n.4515+2T=
XM_011545030.1:c.4515+2T=	XP_011543332.1:n.4515+2T=
XM_011545031.1:c.4515+2T=	XP_011543333.1:n.4515+2T=
XR_949925.1:n.4530+2T=
XR_949926.1:n.4530+2T=
XM_017017735.1:c.2745+2T=	XP_016873224.1:n.2745+2T=
XM_017017736.1:c.2028+2T=	XP_016873225.1:n.2028+2T=
XR_949925.2:n.4530+2T=
XR_949926.2:n.4530+2T=
NM_002335.4:c.4488+2T= MANE Select	NP_002326.2:n.4488+2T=
NM_001291902.2:c.2745+2T=	NP_001278831.1:n.2745+2T=