Canonical Allele Identifier: CA475460827

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68201251G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68433783G>T , CM000673.2:g.68433783G>T	GRCh38
NC_000011.9:g.68201251G>T , CM000673.1:g.68201251G>T	GRCh37
NC_000011.8:g.67957827G>T	NCBI36
NG_015835.1:g.126144G>T
NG_015835.2:g.126144G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.3945G>T MANE Select	ENSP00000294304.6:p.Leu1315=
ENST00000294304.11:c.3945G>T	ENSP00000294304.6:p.Leu1315=
ENST00000529993.5:c.*2551G>T	ENSP00000436652.1:n.*2551G>T
NM_001291902.1:c.2202G>T	NP_001278831.1:p.Leu734=
NM_002335.3:c.3945G>T	NP_002326.2:p.Leu1315=
XM_005273994.2:c.3945G>T	XP_005274051.1:p.Leu1315=
XM_011545029.1:c.3972G>T	XP_011543331.1:p.Leu1324=
XM_011545030.1:c.3972G>T	XP_011543332.1:p.Leu1324=
XM_011545031.1:c.3972G>T	XP_011543333.1:p.Leu1324=
XR_949925.1:n.3987G>T
XR_949926.1:n.3987G>T
XM_017017735.1:c.2202G>T	XP_016873224.1:p.Leu734=
XM_017017736.1:c.1485G>T	XP_016873225.1:p.Leu495=
XR_949925.2:n.3987G>T
XR_949926.2:n.3987G>T
NM_002335.4:c.3945G>T MANE Select	NP_002326.2:p.Leu1315=
NM_001291902.2:c.2202G>T	NP_001278831.1:p.Leu734=