Canonical Allele Identifier: CA1980610921
Gene: LRP5 HGNC NCBI

Linked Data

dbSNP Id: rs634008

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68327273C>A , CM000673.2:g.68327273C>A GRCh38
NC_000011.9:g.68094741C>A , CM000673.1:g.68094741C>A GRCh37
NC_000011.8:g.67851317C>A NCBI36
NG_015835.1:g.19634C>A
NG_015835.2:g.19634C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000294304.12:c.91+14468C>A MANE Select ENSP00000294304.6:n.91+14468C>A
ENST00000294304.11:c.91+14468C>A ENSP00000294304.6:n.91+14468C>A
ENST00000529993.5:c.91+14468C>A ENSP00000436652.1:n.91+14468C>A
NM_001291902.1:c.-1675+14468C>A NP_001278831.1:n.-1675+14468C>A
NM_002335.3:c.91+14468C>A NP_002326.2:n.91+14468C>A
XM_005273994.2:c.91+14468C>A XP_005274051.1:n.91+14468C>A
XM_011545029.1:c.119-20574C>A XP_011543331.1:n.119-20574C>A
XM_011545030.1:c.119-20574C>A XP_011543332.1:n.119-20574C>A
XM_011545031.1:c.119-20574C>A XP_011543333.1:n.119-20574C>A
XR_247245.2:n.2071G>T
XR_949925.1:n.134-20574C>A
XR_949926.1:n.134-20574C>A
XR_001747874.1:n.134-20574C>A
XR_949925.2:n.134-20574C>A
XR_949926.2:n.134-20574C>A
NM_002335.4:c.91+14468C>A MANE Select NP_002326.2:n.91+14468C>A
NM_001291902.2:c.-1675+14468C>A NP_001278831.1:n.-1675+14468C>A