Canonical Allele Identifier: CA10585006
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251316
ClinVar RCV Id: RCV000237334
dbSNP Id: rs879254588

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105506del , CM000681.2:g.11105506del GRCh38
NC_000019.9:g.11216182del , CM000681.1:g.11216182del GRCh37
NC_000019.8:g.11077182del NCBI36
NG_009060.1:g.21126del , LRG_274:g.21126del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.858del ENSP00000252444.6:p.Phe286LeufsTer6
ENST00000559340.2:c.600del ENSP00000453696.2:p.Phe200LeufsTer6
ENST00000560467.2:c.600del ENSP00000453513.2:p.Phe200LeufsTer6
ENST00000558518.6:c.600del MANE Select ENSP00000454071.1:p.Phe200LeufsTer6
ENST00000252444.9:c.854del
ENST00000455727.6:c.314-1886del ENSP00000397829.2:n.314-1886del
ENST00000535915.5:c.477del ENSP00000440520.1:p.Phe159LeufsTer6
ENST00000545707.5:c.314-1059del ENSP00000437639.1:n.314-1059del
ENST00000557933.5:c.600del ENSP00000453557.1:p.Phe200LeufsTer6
ENST00000558013.5:c.600del ENSP00000453346.1:p.Phe200LeufsTer6
ENST00000558518.5:c.600del ENSP00000454071.1:p.Phe200LeufsTer6
ENST00000560467.1:c.200del
NM_000527.4:c.600del , LRG_274t1:c.600del NP_000518.1:p.Phe200LeufsTer6
NM_001195798.1:c.600del NP_001182727.1:p.Phe200LeufsTer6
NM_001195799.1:c.477del NP_001182728.1:p.Phe159LeufsTer6
NM_001195800.1:c.314-1886del NP_001182729.1:n.314-1886del
NM_001195803.1:c.314-1059del NP_001182732.1:n.314-1059del
XM_011528010.1:c.600del XP_011526312.1:p.Phe200LeufsTer6
XM_011528011.1:c.314-1059del XP_011526313.1:n.314-1059del
XR_244074.2:n.750del
XM_011528010.2:c.600del XP_011526312.1:p.Phe200LeufsTer6
XR_001753685.2:n.717del
XR_001753686.2:n.717del
NM_000527.5:c.600del MANE Select NP_000518.1:p.Phe200LeufsTer6
NM_001195798.2:c.600del NP_001182727.1:p.Phe200LeufsTer6
NM_001195799.2:c.477del NP_001182728.1:p.Phe159LeufsTer6
NM_001195800.2:c.314-1886del NP_001182729.1:n.314-1886del
NM_001195803.2:c.314-1059del NP_001182732.1:n.314-1059del