Canonical Allele Identifier: CA645373228
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 430760
ClinVar RCV Id: RCV000495868
dbSNP Id: rs1131692197

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105572_11105594del , CM000681.2:g.11105572_11105594del GRCh38
NC_000019.9:g.11216248_11216270del , CM000681.1:g.11216248_11216270del GRCh37
NC_000019.8:g.11077248_11077270del NCBI36
NG_009060.1:g.21192_21214del , LRG_274:g.21192_21214del

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.924_946del ENSP00000252444.6:p.Cys308Ter
ENST00000559340.2:c.666_688del ENSP00000453696.2:p.Cys222Ter
ENST00000560467.2:c.666_688del ENSP00000453513.2:p.Cys222Ter
ENST00000558518.6:c.666_688del MANE Select ENSP00000454071.1:p.Cys222Ter
ENST00000252444.9:c.920_942del
ENST00000455727.6:c.314-1820_314-1798del ENSP00000397829.2:n.314-1820_314-1798del
ENST00000535915.5:c.543_565del ENSP00000440520.1:p.Cys181Ter
ENST00000545707.5:c.314-993_314-971del ENSP00000437639.1:n.314-993_314-971del
ENST00000557933.5:c.666_688del ENSP00000453557.1:p.Cys222Ter
ENST00000558013.5:c.666_688del ENSP00000453346.1:p.Cys222Ter
ENST00000558518.5:c.666_688del ENSP00000454071.1:p.Cys222Ter
ENST00000560467.1:c.266_288del
NM_000527.4:c.666_688del , LRG_274t1:c.666_688del NP_000518.1:p.Cys222Ter
NM_001195798.1:c.666_688del NP_001182727.1:p.Cys222Ter
NM_001195799.1:c.543_565del NP_001182728.1:p.Cys181Ter
NM_001195800.1:c.314-1820_314-1798del NP_001182729.1:n.314-1820_314-1798del
NM_001195803.1:c.314-993_314-971del NP_001182732.1:n.314-993_314-971del
XM_011528010.1:c.666_688del XP_011526312.1:p.Cys222Ter
XM_011528011.1:c.314-993_314-971del XP_011526313.1:n.314-993_314-971del
XR_244074.2:n.816_838del
XM_011528010.2:c.666_688del XP_011526312.1:p.Cys222Ter
XR_001753685.2:n.783_805del
XR_001753686.2:n.783_805del
NM_000527.5:c.666_688del MANE Select NP_000518.1:p.Cys222Ter
NM_001195798.2:c.666_688del NP_001182727.1:p.Cys222Ter
NM_001195799.2:c.543_565del NP_001182728.1:p.Cys181Ter
NM_001195800.2:c.314-1820_314-1798del NP_001182729.1:n.314-1820_314-1798del
NM_001195803.2:c.314-993_314-971del NP_001182732.1:n.314-993_314-971del