Canonical Allele Identifier: CA2580096433
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 1705272
ClinVar RCV Id: RCV002283589

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113429del , CM000681.2:g.11113429del GRCh38
NC_000019.9:g.11224105del , CM000681.1:g.11224105del GRCh37
NC_000019.8:g.11085105del NCBI36
NG_009060.1:g.29049del , LRG_274:g.29049del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1596del ENSP00000252444.6:p.Ser533ProfsTer4
ENST00000559340.2:c.1338del ENSP00000453696.2:p.Ser447ProfsTer4
ENST00000560467.2:c.1218del ENSP00000453513.2:p.Ser407ProfsTer4
ENST00000558518.6:c.1338del MANE Select ENSP00000454071.1:p.Ser447ProfsTer4
ENST00000252444.9:c.1592del
ENST00000455727.6:c.834del ENSP00000397829.2:p.Ser279ProfsTer4
ENST00000535915.5:c.1215del ENSP00000440520.1:p.Ser406ProfsTer4
ENST00000545707.5:c.957del ENSP00000437639.1:p.Ser320ProfsTer4
ENST00000557933.5:c.1338del ENSP00000453557.1:p.Ser447ProfsTer4
ENST00000558013.5:c.1338del ENSP00000453346.1:p.Ser447ProfsTer4
ENST00000558518.5:c.1338del ENSP00000454071.1:p.Ser447ProfsTer4
ENST00000559340.1:c.59del
ENST00000560173.1:n.337del
ENST00000560467.1:c.818del
NM_000527.4:c.1338del , LRG_274t1:c.1338del NP_000518.1:p.Ser447ProfsTer4
NM_001195798.1:c.1338del NP_001182727.1:p.Ser447ProfsTer4
NM_001195799.1:c.1215del NP_001182728.1:p.Ser406ProfsTer4
NM_001195800.1:c.834del NP_001182729.1:p.Ser279ProfsTer4
NM_001195803.1:c.957del NP_001182732.1:p.Ser320ProfsTer4
XM_011528010.1:c.1338del XP_011526312.1:p.Ser447ProfsTer4
XM_011528011.1:c.957del XP_011526313.1:p.Ser320ProfsTer4
XR_244074.2:n.1488del
XM_011528010.2:c.1338del XP_011526312.1:p.Ser447ProfsTer4
XR_001753685.2:n.1455del
XR_001753686.2:n.1455del
NM_000527.5:c.1338del MANE Select NP_000518.1:p.Ser447ProfsTer4
NM_001195798.2:c.1338del NP_001182727.1:p.Ser447ProfsTer4
NM_001195799.2:c.1215del NP_001182728.1:p.Ser406ProfsTer4
NM_001195800.2:c.834del NP_001182729.1:p.Ser279ProfsTer4
NM_001195803.2:c.957del NP_001182732.1:p.Ser320ProfsTer4