Canonical Allele Identifier: CA2792540143
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403854_68403855insACA , CM000673.2:g.68403854_68403855insACA GRCh38
NC_000011.9:g.68171322_68171323insACA , CM000673.1:g.68171322_68171323insACA GRCh37
NC_000011.8:g.67927898_67927899insACA NCBI36
NG_015835.1:g.96215_96216insACA
NG_015835.2:g.96215_96216insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1801+155_1801+156insACA MANE Select ENSP00000294304.6:n.1801+155_1801+156insACA
ENST00000294304.11:c.1801+155_1801+156insACA ENSP00000294304.6:n.1801+155_1801+156insACA
ENST00000529993.5:c.*213+155_*213+156insACA ENSP00000436652.1:n.*213+155_*213+156insACA
NM_001291902.1:c.-137+155_-137+156insACA NP_001278831.1:n.-137+155_-137+156insACA
NM_002335.3:c.1801+155_1801+156insACA NP_002326.2:n.1801+155_1801+156insACA
XM_005273994.2:c.1801+155_1801+156insACA XP_005274051.1:n.1801+155_1801+156insACA
XM_011545029.1:c.1828+155_1828+156insACA XP_011543331.1:n.1828+155_1828+156insACA
XM_011545030.1:c.1828+155_1828+156insACA XP_011543332.1:n.1828+155_1828+156insACA
XM_011545031.1:c.1828+155_1828+156insACA XP_011543333.1:n.1828+155_1828+156insACA
XR_949925.1:n.1843+155_1843+156insACA
XR_949926.1:n.1843+155_1843+156insACA
XR_001747874.1:n.1843+155_1843+156insACA
XR_949925.2:n.1843+155_1843+156insACA
XR_949926.2:n.1843+155_1843+156insACA
NM_002335.4:c.1801+155_1801+156insACA MANE Select NP_002326.2:n.1801+155_1801+156insACA
NM_001291902.2:c.-137+155_-137+156insACA NP_001278831.1:n.-137+155_-137+156insACA