Canonical Allele Identifier: CA381613204
Community Standard Title: NM_002335.4(LRP5):c.1532A>C (p.Asp511Ala)
Gene: LRP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68390000A>C , CM000673.2:g.68390000A>C GRCh38
NC_000011.9:g.68157468A>C , CM000673.1:g.68157468A>C GRCh37
NC_000011.8:g.67914044A>C NCBI36
NG_015835.1:g.82361A>C
NG_015835.2:g.82361A>C

Transcript Alleles

HGVS Amino-acid Change
NM_002335.4:c.1532A>C MANE Select NP_002326.2:p.Asp511Ala
ENST00000294304.12:c.1532A>C MANE Select ENSP00000294304.6:p.Asp511Ala
NM_001291902.1:c.-354+3288A>C NP_001278831.1:n.-354+3288A>C
NM_001291902.2:c.-354+3288A>C NP_001278831.1:n.-354+3288A>C
NM_002335.3:c.1532A>C NP_002326.2:p.Asp511Ala
ENST00000294304.11:c.1532A>C ENSP00000294304.6:p.Asp511Ala
ENST00000529993.5:c.1412+3288A>C ENSP00000436652.1:n.1412+3288A>C
XM_005273994.2:c.1532A>C XP_005274051.1:p.Asp511Ala
XM_011545029.1:c.1559A>C XP_011543331.1:p.Asp520Ala
XM_011545030.1:c.1559A>C XP_011543332.1:p.Asp520Ala
XM_011545031.1:c.1559A>C XP_011543333.1:p.Asp520Ala
XR_001747874.1:n.1574A>C
XR_949925.1:n.1574A>C
XR_949925.2:n.1574A>C
XR_949926.1:n.1574A>C
XR_949926.2:n.1574A>C