Canonical Allele Identifier: CA2792540178
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403895_68403896insACT , CM000673.2:g.68403895_68403896insACT GRCh38
NC_000011.9:g.68171363_68171364insACT , CM000673.1:g.68171363_68171364insACT GRCh37
NC_000011.8:g.67927939_67927940insACT NCBI36
NG_015835.1:g.96256_96257insACT
NG_015835.2:g.96256_96257insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1801+196_1801+197insACT MANE Select ENSP00000294304.6:n.1801+196_1801+197insACT
ENST00000294304.11:c.1801+196_1801+197insACT ENSP00000294304.6:n.1801+196_1801+197insACT
ENST00000529993.5:c.*213+196_*213+197insACT ENSP00000436652.1:n.*213+196_*213+197insACT
NM_001291902.1:c.-137+196_-137+197insACT NP_001278831.1:n.-137+196_-137+197insACT
NM_002335.3:c.1801+196_1801+197insACT NP_002326.2:n.1801+196_1801+197insACT
XM_005273994.2:c.1801+196_1801+197insACT XP_005274051.1:n.1801+196_1801+197insACT
XM_011545029.1:c.1828+196_1828+197insACT XP_011543331.1:n.1828+196_1828+197insACT
XM_011545030.1:c.1828+196_1828+197insACT XP_011543332.1:n.1828+196_1828+197insACT
XM_011545031.1:c.1828+196_1828+197insACT XP_011543333.1:n.1828+196_1828+197insACT
XR_949925.1:n.1843+196_1843+197insACT
XR_949926.1:n.1843+196_1843+197insACT
XR_001747874.1:n.1843+196_1843+197insACT
XR_949925.2:n.1843+196_1843+197insACT
XR_949926.2:n.1843+196_1843+197insACT
NM_002335.4:c.1801+196_1801+197insACT MANE Select NP_002326.2:n.1801+196_1801+197insACT
NM_001291902.2:c.-137+196_-137+197insACT NP_001278831.1:n.-137+196_-137+197insACT