Canonical Allele Identifier: CA2792540151
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403864_68403865insAGA , CM000673.2:g.68403864_68403865insAGA GRCh38
NC_000011.9:g.68171332_68171333insAGA , CM000673.1:g.68171332_68171333insAGA GRCh37
NC_000011.8:g.67927908_67927909insAGA NCBI36
NG_015835.1:g.96225_96226insAGA
NG_015835.2:g.96225_96226insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1801+165_1801+166insAGA MANE Select ENSP00000294304.6:n.1801+165_1801+166insAGA
ENST00000294304.11:c.1801+165_1801+166insAGA ENSP00000294304.6:n.1801+165_1801+166insAGA
ENST00000529993.5:c.*213+165_*213+166insAGA ENSP00000436652.1:n.*213+165_*213+166insAGA
NM_001291902.1:c.-137+165_-137+166insAGA NP_001278831.1:n.-137+165_-137+166insAGA
NM_002335.3:c.1801+165_1801+166insAGA NP_002326.2:n.1801+165_1801+166insAGA
XM_005273994.2:c.1801+165_1801+166insAGA XP_005274051.1:n.1801+165_1801+166insAGA
XM_011545029.1:c.1828+165_1828+166insAGA XP_011543331.1:n.1828+165_1828+166insAGA
XM_011545030.1:c.1828+165_1828+166insAGA XP_011543332.1:n.1828+165_1828+166insAGA
XM_011545031.1:c.1828+165_1828+166insAGA XP_011543333.1:n.1828+165_1828+166insAGA
XR_949925.1:n.1843+165_1843+166insAGA
XR_949926.1:n.1843+165_1843+166insAGA
XR_001747874.1:n.1843+165_1843+166insAGA
XR_949925.2:n.1843+165_1843+166insAGA
XR_949926.2:n.1843+165_1843+166insAGA
NM_002335.4:c.1801+165_1801+166insAGA MANE Select NP_002326.2:n.1801+165_1801+166insAGA
NM_001291902.2:c.-137+165_-137+166insAGA NP_001278831.1:n.-137+165_-137+166insAGA