Canonical Allele Identifier: CA10585670
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 252100
ClinVar RCV Id: RCV000238112
dbSNP Id: rs879255065

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120122del , CM000681.2:g.11120122del GRCh38
NC_000019.9:g.11230798del , CM000681.1:g.11230798del GRCh37
NC_000019.8:g.11091798del NCBI36
NG_009060.1:g.35742del , LRG_274:g.35742del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2134del ENSP00000252444.6:p.Glu712LysfsTer?
ENST00000559340.2:c.1736del ENSP00000453696.2:p.Arg579GlnfsTer?
ENST00000560467.2:c.1756del ENSP00000453513.2:p.Glu586LysfsTer?
ENST00000558518.6:c.1876del MANE Select ENSP00000454071.1:p.Glu626LysfsTer?
ENST00000252444.9:c.2130del
ENST00000455727.6:c.1372del ENSP00000397829.2:p.Glu458LysfsTer?
ENST00000535915.5:c.1753del ENSP00000440520.1:p.Glu585LysfsTer?
ENST00000545707.5:c.1495del ENSP00000437639.1:p.Glu499LysfsTer?
ENST00000557933.5:c.1876del ENSP00000453557.1:p.Glu626LysfsTer?
ENST00000558013.5:c.1876del ENSP00000453346.1:p.Glu626LysfsTer?
ENST00000558518.5:c.1876del ENSP00000454071.1:p.Glu626LysfsTer?
ENST00000559340.1:c.457del
NM_000527.4:c.1876del , LRG_274t1:c.1876del NP_000518.1:p.Glu626LysfsTer?
NM_001195798.1:c.1876del NP_001182727.1:p.Glu626LysfsTer?
NM_001195799.1:c.1753del NP_001182728.1:p.Glu585LysfsTer?
NM_001195800.1:c.1372del NP_001182729.1:p.Glu458LysfsTer?
NM_001195803.1:c.1495del NP_001182732.1:p.Glu499LysfsTer?
XM_011528010.1:c.1876del XP_011526312.1:p.Glu626LysfsTer?
XM_011528011.1:c.1495del XP_011526313.1:p.Glu499LysfsTer?
XR_244074.2:n.1886del
XM_011528010.2:c.1876del XP_011526312.1:p.Glu626LysfsTer?
XR_001753685.2:n.1993del
XR_001753686.2:n.1853del
NM_000527.5:c.1876del MANE Select NP_000518.1:p.Glu626LysfsTer?
NM_001195798.2:c.1876del NP_001182727.1:p.Glu626LysfsTer?
NM_001195799.2:c.1753del NP_001182728.1:p.Glu585LysfsTer?
NM_001195800.2:c.1372del NP_001182729.1:p.Glu458LysfsTer?
NM_001195803.2:c.1495del NP_001182732.1:p.Glu499LysfsTer?