Canonical Allele Identifier: CA10585259
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251607
ClinVar RCV Id: RCV000237912
dbSNP Id: rs879254761

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110742del , CM000681.2:g.11110742del GRCh38
NC_000019.9:g.11221418del , CM000681.1:g.11221418del GRCh37
NC_000019.8:g.11082418del NCBI36
NG_009060.1:g.26362del , LRG_274:g.26362del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1289del ENSP00000252444.6:p.Phe430SerfsTer26
ENST00000559340.2:c.1031del ENSP00000453696.2:p.Phe344SerfsTer26
ENST00000560467.2:c.941-772del ENSP00000453513.2:n.941-772del
ENST00000558518.6:c.1031del MANE Select ENSP00000454071.1:p.Phe344SerfsTer26
ENST00000252444.9:c.1285del
ENST00000455727.6:c.527del ENSP00000397829.2:p.Phe176SerfsTer26
ENST00000535915.5:c.908del ENSP00000440520.1:p.Phe303SerfsTer26
ENST00000545707.5:c.650del ENSP00000437639.1:p.Phe217SerfsTer26
ENST00000557933.5:c.1031del ENSP00000453557.1:p.Phe344SerfsTer26
ENST00000558013.5:c.1031del ENSP00000453346.1:p.Phe344SerfsTer26
ENST00000558518.5:c.1031del ENSP00000454071.1:p.Phe344SerfsTer26
ENST00000560173.1:n.30del
ENST00000560467.1:c.541-772del
NM_000527.4:c.1031del , LRG_274t1:c.1031del NP_000518.1:p.Phe344SerfsTer26
NM_001195798.1:c.1031del NP_001182727.1:p.Phe344SerfsTer26
NM_001195799.1:c.908del NP_001182728.1:p.Phe303SerfsTer26
NM_001195800.1:c.527del NP_001182729.1:p.Phe176SerfsTer26
NM_001195803.1:c.650del NP_001182732.1:p.Phe217SerfsTer26
XM_011528010.1:c.1031del XP_011526312.1:p.Phe344SerfsTer26
XM_011528011.1:c.650del XP_011526313.1:p.Phe217SerfsTer26
XR_244074.2:n.1181del
XM_011528010.2:c.1031del XP_011526312.1:p.Phe344SerfsTer26
XR_001753685.2:n.1148del
XR_001753686.2:n.1148del
NM_000527.5:c.1031del MANE Select NP_000518.1:p.Phe344SerfsTer26
NM_001195798.2:c.1031del NP_001182727.1:p.Phe344SerfsTer26
NM_001195799.2:c.908del NP_001182728.1:p.Phe303SerfsTer26
NM_001195800.2:c.527del NP_001182729.1:p.Phe176SerfsTer26
NM_001195803.2:c.650del NP_001182732.1:p.Phe217SerfsTer26