Canonical Allele Identifier: CA915952546
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 2843694
ClinVar RCV Id: RCV003742085
dbSNP Id: rs1600727285

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113550_11113558del , CM000681.2:g.11113550_11113558del GRCh38
NC_000019.9:g.11224226_11224234del , CM000681.1:g.11224226_11224234del GRCh37
NC_000019.8:g.11085226_11085234del NCBI36
NG_009060.1:g.29170_29178del , LRG_274:g.29170_29178del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1632_1640del ENSP00000252444.6:p.Arg544_Gly547delinsSer
ENST00000559340.2:c.1374_1382del ENSP00000453696.2:p.Arg458_Gly461delinsSer
ENST00000560467.2:c.1254_1262del ENSP00000453513.2:p.Arg418_Gly421delinsSer
ENST00000558518.6:c.1374_1382del MANE Select ENSP00000454071.1:p.Arg458_Gly461delinsSer
ENST00000252444.9:c.1628_1636del
ENST00000455727.6:c.870_878del ENSP00000397829.2:p.Arg290_Gly293delinsSer
ENST00000535915.5:c.1251_1259del ENSP00000440520.1:p.Arg417_Gly420delinsSer
ENST00000545707.5:c.993_1001del ENSP00000437639.1:p.Arg331_Gly334delinsSer
ENST00000557933.5:c.1374_1382del ENSP00000453557.1:p.Arg458_Gly461delinsSer
ENST00000558013.5:c.1374_1382del ENSP00000453346.1:p.Arg458_Gly461delinsSer
ENST00000558518.5:c.1374_1382del ENSP00000454071.1:p.Arg458_Gly461delinsSer
ENST00000559340.1:c.95_103del
ENST00000560467.1:c.854_862del
NM_000527.4:c.1374_1382del , LRG_274t1:c.1374_1382del NP_000518.1:p.Arg458_Gly461delinsSer
NM_001195798.1:c.1374_1382del NP_001182727.1:p.Arg458_Gly461delinsSer
NM_001195799.1:c.1251_1259del NP_001182728.1:p.Arg417_Gly420delinsSer
NM_001195800.1:c.870_878del NP_001182729.1:p.Arg290_Gly293delinsSer
NM_001195803.1:c.993_1001del NP_001182732.1:p.Arg331_Gly334delinsSer
XM_011528010.1:c.1374_1382del XP_011526312.1:p.Arg458_Gly461delinsSer
XM_011528011.1:c.993_1001del XP_011526313.1:p.Arg331_Gly334delinsSer
XR_244074.2:n.1524_1532del
XM_011528010.2:c.1374_1382del XP_011526312.1:p.Arg458_Gly461delinsSer
XR_001753685.2:n.1491_1499del
XR_001753686.2:n.1491_1499del
NM_000527.5:c.1374_1382del MANE Select NP_000518.1:p.Arg458_Gly461delinsSer
NM_001195798.2:c.1374_1382del NP_001182727.1:p.Arg458_Gly461delinsSer
NM_001195799.2:c.1251_1259del NP_001182728.1:p.Arg417_Gly420delinsSer
NM_001195800.2:c.870_878del NP_001182729.1:p.Arg290_Gly293delinsSer
NM_001195803.2:c.993_1001del NP_001182732.1:p.Arg331_Gly334delinsSer