Canonical Allele Identifier: CA2543345393
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403797_68403798insGT , CM000673.2:g.68403797_68403798insGT GRCh38
NC_000011.9:g.68171265_68171266insGT , CM000673.1:g.68171265_68171266insGT GRCh37
NC_000011.8:g.67927841_67927842insGT NCBI36
NG_015835.1:g.96158_96159insGT
NG_015835.2:g.96158_96159insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1801+98_1801+99insGT MANE Select ENSP00000294304.6:n.1801+98_1801+99insGT
ENST00000294304.11:c.1801+98_1801+99insGT ENSP00000294304.6:n.1801+98_1801+99insGT
ENST00000529993.5:c.*213+98_*213+99insGT ENSP00000436652.1:n.*213+98_*213+99insGT
NM_001291902.1:c.-137+98_-137+99insGT NP_001278831.1:n.-137+98_-137+99insGT
NM_002335.3:c.1801+98_1801+99insGT NP_002326.2:n.1801+98_1801+99insGT
XM_005273994.2:c.1801+98_1801+99insGT XP_005274051.1:n.1801+98_1801+99insGT
XM_011545029.1:c.1828+98_1828+99insGT XP_011543331.1:n.1828+98_1828+99insGT
XM_011545030.1:c.1828+98_1828+99insGT XP_011543332.1:n.1828+98_1828+99insGT
XM_011545031.1:c.1828+98_1828+99insGT XP_011543333.1:n.1828+98_1828+99insGT
XR_949925.1:n.1843+98_1843+99insGT
XR_949926.1:n.1843+98_1843+99insGT
XR_001747874.1:n.1843+98_1843+99insGT
XR_949925.2:n.1843+98_1843+99insGT
XR_949926.2:n.1843+98_1843+99insGT
NM_002335.4:c.1801+98_1801+99insGT MANE Select NP_002326.2:n.1801+98_1801+99insGT
NM_001291902.2:c.-137+98_-137+99insGT NP_001278831.1:n.-137+98_-137+99insGT