Canonical Allele Identifier: CA10585181
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251509
ClinVar RCV Id: RCV000237246
dbSNP Id: rs879254712

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107470del , CM000681.2:g.11107470del GRCh38
NC_000019.9:g.11218146del , CM000681.1:g.11218146del GRCh37
NC_000019.8:g.11079146del NCBI36
NG_009060.1:g.23090del , LRG_274:g.23090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1154del ENSP00000252444.6:p.Ala385ValfsTer?
ENST00000559340.2:c.896del ENSP00000453696.2:p.Ala299ValfsTer?
ENST00000560467.2:c.896del ENSP00000453513.2:p.Ala299ValfsTer?
ENST00000558518.6:c.896del MANE Select ENSP00000454071.1:p.Ala299ValfsTer?
ENST00000252444.9:c.1150del
ENST00000455727.6:c.392del ENSP00000397829.2:p.Ala131ValfsTer?
ENST00000535915.5:c.773del ENSP00000440520.1:p.Ala258ValfsTer?
ENST00000545707.5:c.515del ENSP00000437639.1:p.Ala172ValfsTer?
ENST00000557933.5:c.896del ENSP00000453557.1:p.Ala299ValfsTer?
ENST00000558013.5:c.896del ENSP00000453346.1:p.Ala299ValfsTer?
ENST00000558518.5:c.896del ENSP00000454071.1:p.Ala299ValfsTer?
ENST00000558528.1:n.411del
ENST00000560467.1:c.496del
NM_000527.4:c.896del , LRG_274t1:c.896del NP_000518.1:p.Ala299ValfsTer?
NM_001195798.1:c.896del NP_001182727.1:p.Ala299ValfsTer?
NM_001195799.1:c.773del NP_001182728.1:p.Ala258ValfsTer?
NM_001195800.1:c.392del NP_001182729.1:p.Ala131ValfsTer?
NM_001195803.1:c.515del NP_001182732.1:p.Ala172ValfsTer?
XM_011528010.1:c.896del XP_011526312.1:p.Ala299ValfsTer?
XM_011528011.1:c.515del XP_011526313.1:p.Ala172ValfsTer?
XR_244074.2:n.1046del
XM_011528010.2:c.896del XP_011526312.1:p.Ala299ValfsTer?
XR_001753685.2:n.1013del
XR_001753686.2:n.1013del
NM_000527.5:c.896del MANE Select NP_000518.1:p.Ala299ValfsTer?
NM_001195798.2:c.896del NP_001182727.1:p.Ala299ValfsTer?
NM_001195799.2:c.773del NP_001182728.1:p.Ala258ValfsTer?
NM_001195800.2:c.392del NP_001182729.1:p.Ala131ValfsTer?
NM_001195803.2:c.515del NP_001182732.1:p.Ala172ValfsTer?