Canonical Allele Identifier: CA2792540146
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403857_68403858insTC , CM000673.2:g.68403857_68403858insTC GRCh38
NC_000011.9:g.68171325_68171326insTC , CM000673.1:g.68171325_68171326insTC GRCh37
NC_000011.8:g.67927901_67927902insTC NCBI36
NG_015835.1:g.96218_96219insTC
NG_015835.2:g.96218_96219insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1801+158_1801+159insTC MANE Select ENSP00000294304.6:n.1801+158_1801+159insTC
ENST00000294304.11:c.1801+158_1801+159insTC ENSP00000294304.6:n.1801+158_1801+159insTC
ENST00000529993.5:c.*213+158_*213+159insTC ENSP00000436652.1:n.*213+158_*213+159insTC
NM_001291902.1:c.-137+158_-137+159insTC NP_001278831.1:n.-137+158_-137+159insTC
NM_002335.3:c.1801+158_1801+159insTC NP_002326.2:n.1801+158_1801+159insTC
XM_005273994.2:c.1801+158_1801+159insTC XP_005274051.1:n.1801+158_1801+159insTC
XM_011545029.1:c.1828+158_1828+159insTC XP_011543331.1:n.1828+158_1828+159insTC
XM_011545030.1:c.1828+158_1828+159insTC XP_011543332.1:n.1828+158_1828+159insTC
XM_011545031.1:c.1828+158_1828+159insTC XP_011543333.1:n.1828+158_1828+159insTC
XR_949925.1:n.1843+158_1843+159insTC
XR_949926.1:n.1843+158_1843+159insTC
XR_001747874.1:n.1843+158_1843+159insTC
XR_949925.2:n.1843+158_1843+159insTC
XR_949926.2:n.1843+158_1843+159insTC
NM_002335.4:c.1801+158_1801+159insTC MANE Select NP_002326.2:n.1801+158_1801+159insTC
NM_001291902.2:c.-137+158_-137+159insTC NP_001278831.1:n.-137+158_-137+159insTC