Canonical Allele Identifier: CA381613755

Gene: LRP5

Linked Data

• MyVariant Identifiers: chr11:g.68201157C>T (hg19) ; chr11:g.68433689C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68433689C>T , CM000673.2:g.68433689C>T	GRCh38
NC_000011.9:g.68201157C>T , CM000673.1:g.68201157C>T	GRCh37
NC_000011.8:g.67957733C>T	NCBI36
NG_015835.1:g.126050C>T
NG_015835.2:g.126050C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.3851C>T MANE Select	ENSP00000294304.6:p.Pro1284Leu
ENST00000294304.11:c.3851C>T	ENSP00000294304.6:p.Pro1284Leu
ENST00000529993.5:c.*2457C>T	ENSP00000436652.1:n.*2457C>T
NM_001291902.1:c.2108C>T	NP_001278831.1:p.Pro703Leu
NM_002335.3:c.3851C>T	NP_002326.2:p.Pro1284Leu
XM_005273994.2:c.3851C>T	XP_005274051.1:p.Pro1284Leu
XM_011545029.1:c.3878C>T	XP_011543331.1:p.Pro1293Leu
XM_011545030.1:c.3878C>T	XP_011543332.1:p.Pro1293Leu
XM_011545031.1:c.3878C>T	XP_011543333.1:p.Pro1293Leu
XR_949925.1:n.3893C>T
XR_949926.1:n.3893C>T
XM_017017735.1:c.2108C>T	XP_016873224.1:p.Pro703Leu
XM_017017736.1:c.1391C>T	XP_016873225.1:p.Pro464Leu
XR_949925.2:n.3893C>T
XR_949926.2:n.3893C>T
NM_002335.4:c.3851C>T MANE Select	NP_002326.2:p.Pro1284Leu
NM_001291902.2:c.2108C>T	NP_001278831.1:p.Pro703Leu