Canonical Allele Identifier: CA2792540123
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68403830_68403831insA , CM000673.2:g.68403830_68403831insA GRCh38
NC_000011.9:g.68171298_68171299insA , CM000673.1:g.68171298_68171299insA GRCh37
NC_000011.8:g.67927874_67927875insA NCBI36
NG_015835.1:g.96191_96192insA
NG_015835.2:g.96191_96192insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000294304.12:c.1801+131_1801+132insA MANE Select ENSP00000294304.6:n.1801+131_1801+132insA
ENST00000294304.11:c.1801+131_1801+132insA ENSP00000294304.6:n.1801+131_1801+132insA
ENST00000529993.5:c.*213+131_*213+132insA ENSP00000436652.1:n.*213+131_*213+132insA
NM_001291902.1:c.-137+131_-137+132insA NP_001278831.1:n.-137+131_-137+132insA
NM_002335.3:c.1801+131_1801+132insA NP_002326.2:n.1801+131_1801+132insA
XM_005273994.2:c.1801+131_1801+132insA XP_005274051.1:n.1801+131_1801+132insA
XM_011545029.1:c.1828+131_1828+132insA XP_011543331.1:n.1828+131_1828+132insA
XM_011545030.1:c.1828+131_1828+132insA XP_011543332.1:n.1828+131_1828+132insA
XM_011545031.1:c.1828+131_1828+132insA XP_011543333.1:n.1828+131_1828+132insA
XR_949925.1:n.1843+131_1843+132insA
XR_949926.1:n.1843+131_1843+132insA
XR_001747874.1:n.1843+131_1843+132insA
XR_949925.2:n.1843+131_1843+132insA
XR_949926.2:n.1843+131_1843+132insA
NM_002335.4:c.1801+131_1801+132insA MANE Select NP_002326.2:n.1801+131_1801+132insA
NM_001291902.2:c.-137+131_-137+132insA NP_001278831.1:n.-137+131_-137+132insA