Canonical Allele Identifier: CA1980622262

Gene: LRP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68433727G= , CM000673.2:g.68433727G=	GRCh38
NC_000011.9:g.68201195G= , CM000673.1:g.68201195G=	GRCh37
NC_000011.8:g.67957771G=	NCBI36
NG_015835.1:g.126088G=
NG_015835.2:g.126088G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294304.12:c.3889G= MANE Select	ENSP00000294304.6:p.Val1297=
ENST00000294304.11:c.3889G=	ENSP00000294304.6:p.Val1297=
ENST00000529993.5:c.*2495G=	ENSP00000436652.1:n.*2495G=
NM_001291902.1:c.2146G=	NP_001278831.1:p.Val716=
NM_002335.3:c.3889G=	NP_002326.2:p.Val1297=
XM_005273994.2:c.3889G=	XP_005274051.1:p.Val1297=
XM_011545029.1:c.3916G=	XP_011543331.1:p.Val1306=
XM_011545030.1:c.3916G=	XP_011543332.1:p.Val1306=
XM_011545031.1:c.3916G=	XP_011543333.1:p.Val1306=
XR_949925.1:n.3931G=
XR_949926.1:n.3931G=
XM_017017735.1:c.2146G=	XP_016873224.1:p.Val716=
XM_017017736.1:c.1429G=	XP_016873225.1:p.Val477=
XR_949925.2:n.3931G=
XR_949926.2:n.3931G=
NM_002335.4:c.3889G= MANE Select	NP_002326.2:p.Val1297=
NM_001291902.2:c.2146G=	NP_001278831.1:p.Val716=