Canonical Allele Identifier: CA10585358
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251734
ClinVar RCV Id: RCV000237611
dbSNP Id: rs879254833

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113300del , CM000681.2:g.11113300del GRCh38
NC_000019.9:g.11223976del , CM000681.1:g.11223976del GRCh37
NC_000019.8:g.11084976del NCBI36
NG_009060.1:g.28920del , LRG_274:g.28920del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1467del ENSP00000252444.6:p.Phe489LeufsTer10
ENST00000559340.2:c.1209del ENSP00000453696.2:p.Phe403LeufsTer10
ENST00000560467.2:c.1089del ENSP00000453513.2:p.Phe363LeufsTer10
ENST00000558518.6:c.1209del MANE Select ENSP00000454071.1:p.Phe403LeufsTer10
ENST00000252444.9:c.1463del
ENST00000455727.6:c.705del ENSP00000397829.2:p.Phe235LeufsTer10
ENST00000535915.5:c.1086del ENSP00000440520.1:p.Phe362LeufsTer10
ENST00000545707.5:c.828del ENSP00000437639.1:p.Phe276LeufsTer10
ENST00000557933.5:c.1209del ENSP00000453557.1:p.Phe403LeufsTer10
ENST00000558013.5:c.1209del ENSP00000453346.1:p.Phe403LeufsTer10
ENST00000558518.5:c.1209del ENSP00000454071.1:p.Phe403LeufsTer10
ENST00000560173.1:n.208del
ENST00000560467.1:c.689del
NM_000527.4:c.1209del , LRG_274t1:c.1209del NP_000518.1:p.Phe403LeufsTer10
NM_001195798.1:c.1209del NP_001182727.1:p.Phe403LeufsTer10
NM_001195799.1:c.1086del NP_001182728.1:p.Phe362LeufsTer10
NM_001195800.1:c.705del NP_001182729.1:p.Phe235LeufsTer10
NM_001195803.1:c.828del NP_001182732.1:p.Phe276LeufsTer10
XM_011528010.1:c.1209del XP_011526312.1:p.Phe403LeufsTer10
XM_011528011.1:c.828del XP_011526313.1:p.Phe276LeufsTer10
XR_244074.2:n.1359del
XM_011528010.2:c.1209del XP_011526312.1:p.Phe403LeufsTer10
XR_001753685.2:n.1326del
XR_001753686.2:n.1326del
NM_000527.5:c.1209del MANE Select NP_000518.1:p.Phe403LeufsTer10
NM_001195798.2:c.1209del NP_001182727.1:p.Phe403LeufsTer10
NM_001195799.2:c.1086del NP_001182728.1:p.Phe362LeufsTer10
NM_001195800.2:c.705del NP_001182729.1:p.Phe235LeufsTer10
NM_001195803.2:c.828del NP_001182732.1:p.Phe276LeufsTer10