Canonical Allele Identifier: CA224266971

Gene: LRP5

Linked Data

• dbSNP Id: rs34813266
• MyVariant Identifiers: chr11:g.68171346_68171347insA (hg19) ; chr11:g.68403878_68403879insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68403879dup , CM000673.2:g.68403879dup	GRCh38
NC_000011.9:g.68171347dup , CM000673.1:g.68171347dup	GRCh37
NC_000011.8:g.67927923dup	NCBI36
NG_015835.1:g.96240dup
NG_015835.2:g.96240dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294304.12:c.1801+180dup MANE Select	ENSP00000294304.6:n.1801+180dup
ENST00000294304.11:c.1801+180dup	ENSP00000294304.6:n.1801+180dup
ENST00000529993.5:c.*213+180dup	ENSP00000436652.1:n.*213+180dup
NM_001291902.1:c.-137+180dup	NP_001278831.1:n.-137+180dup
NM_002335.3:c.1801+180dup	NP_002326.2:n.1801+180dup
XM_005273994.2:c.1801+180dup	XP_005274051.1:n.1801+180dup
XM_011545029.1:c.1828+180dup	XP_011543331.1:n.1828+180dup
XM_011545030.1:c.1828+180dup	XP_011543332.1:n.1828+180dup
XM_011545031.1:c.1828+180dup	XP_011543333.1:n.1828+180dup
XR_949925.1:n.1843+180dup
XR_949926.1:n.1843+180dup
XR_001747874.1:n.1843+180dup
XR_949925.2:n.1843+180dup
XR_949926.2:n.1843+180dup
NM_002335.4:c.1801+180dup MANE Select	NP_002326.2:n.1801+180dup
NM_001291902.2:c.-137+180dup	NP_001278831.1:n.-137+180dup