Canonical Allele Identifier: CA10585395
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251777
dbSNP Id: rs879254858

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113397del , CM000681.2:g.11113397del GRCh38
NC_000019.9:g.11224073del , CM000681.1:g.11224073del GRCh37
NC_000019.8:g.11085073del NCBI36
NG_009060.1:g.29017del , LRG_274:g.29017del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1564del ENSP00000252444.6:p.Val522TrpfsTer15
ENST00000559340.2:c.1306del ENSP00000453696.2:p.Val436TrpfsTer15
ENST00000560467.2:c.1186del ENSP00000453513.2:p.Val396TrpfsTer15
ENST00000558518.6:c.1306del MANE Select ENSP00000454071.1:p.Val436TrpfsTer15
ENST00000252444.9:c.1560del
ENST00000455727.6:c.802del ENSP00000397829.2:p.Val268TrpfsTer15
ENST00000535915.5:c.1183del ENSP00000440520.1:p.Val395TrpfsTer15
ENST00000545707.5:c.925del ENSP00000437639.1:p.Val309TrpfsTer15
ENST00000557933.5:c.1306del ENSP00000453557.1:p.Val436TrpfsTer15
ENST00000558013.5:c.1306del ENSP00000453346.1:p.Val436TrpfsTer15
ENST00000558518.5:c.1306del ENSP00000454071.1:p.Val436TrpfsTer15
ENST00000559340.1:c.27del
ENST00000560173.1:n.305del
ENST00000560467.1:c.786del
NM_000527.4:c.1306del , LRG_274t1:c.1306del NP_000518.1:p.Val436TrpfsTer15
NM_001195798.1:c.1306del NP_001182727.1:p.Val436TrpfsTer15
NM_001195799.1:c.1183del NP_001182728.1:p.Val395TrpfsTer15
NM_001195800.1:c.802del NP_001182729.1:p.Val268TrpfsTer15
NM_001195803.1:c.925del NP_001182732.1:p.Val309TrpfsTer15
XM_011528010.1:c.1306del XP_011526312.1:p.Val436TrpfsTer15
XM_011528011.1:c.925del XP_011526313.1:p.Val309TrpfsTer15
XR_244074.2:n.1456del
XM_011528010.2:c.1306del XP_011526312.1:p.Val436TrpfsTer15
XR_001753685.2:n.1423del
XR_001753686.2:n.1423del
NM_000527.5:c.1306del MANE Select NP_000518.1:p.Val436TrpfsTer15
NM_001195798.2:c.1306del NP_001182727.1:p.Val436TrpfsTer15
NM_001195799.2:c.1183del NP_001182728.1:p.Val395TrpfsTer15
NM_001195800.2:c.802del NP_001182729.1:p.Val268TrpfsTer15
NM_001195803.2:c.925del NP_001182732.1:p.Val309TrpfsTer15