Canonical Allele Identifier: CA381616710
Gene: LRP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68410125T>C , CM000673.2:g.68410125T>C GRCh38
NC_000011.9:g.68177593T>C , CM000673.1:g.68177593T>C GRCh37
NC_000011.8:g.67934169T>C NCBI36
NG_015835.1:g.102486T>C
NG_015835.2:g.102486T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.2303T>C MANE Select ENSP00000294304.6:p.Leu768Pro
ENST00000294304.11:c.2303T>C ENSP00000294304.6:p.Leu768Pro
ENST00000528714.1:n.97T>C
ENST00000529993.5:c.*909T>C ENSP00000436652.1:n.*909T>C
NM_001291902.1:c.560T>C NP_001278831.1:p.Leu187Pro
NM_002335.3:c.2303T>C NP_002326.2:p.Leu768Pro
XM_005273994.2:c.2303T>C XP_005274051.1:p.Leu768Pro
XM_011545029.1:c.2330T>C XP_011543331.1:p.Leu777Pro
XM_011545030.1:c.2330T>C XP_011543332.1:p.Leu777Pro
XM_011545031.1:c.2330T>C XP_011543333.1:p.Leu777Pro
XR_949925.1:n.2345T>C
XR_949926.1:n.2345T>C
XM_017017735.1:c.560T>C XP_016873224.1:p.Leu187Pro
XR_001747874.1:n.2345T>C
XR_949925.2:n.2345T>C
XR_949926.2:n.2345T>C
NM_002335.4:c.2303T>C MANE Select NP_002326.2:p.Leu768Pro
NM_001291902.2:c.560T>C NP_001278831.1:p.Leu187Pro