Canonical Allele Identifier: CA10585233
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251579
ClinVar RCV Id: RCV000237714
dbSNP Id: rs879254745

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110682del , CM000681.2:g.11110682del GRCh38
NC_000019.9:g.11221358del , CM000681.1:g.11221358del GRCh37
NC_000019.8:g.11082358del NCBI36
NG_009060.1:g.26302del , LRG_274:g.26302del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1229del ENSP00000252444.6:p.Gly410AlafsTer?
ENST00000559340.2:c.971del ENSP00000453696.2:p.Gly324AlafsTer?
ENST00000560467.2:c.941-832del ENSP00000453513.2:n.941-832del
ENST00000558518.6:c.971del MANE Select ENSP00000454071.1:p.Gly324AlafsTer?
ENST00000252444.9:c.1225del
ENST00000455727.6:c.467del ENSP00000397829.2:p.Gly156AlafsTer?
ENST00000535915.5:c.848del ENSP00000440520.1:p.Gly283AlafsTer?
ENST00000545707.5:c.590del ENSP00000437639.1:p.Gly197AlafsTer?
ENST00000557933.5:c.971del ENSP00000453557.1:p.Gly324AlafsTer?
ENST00000558013.5:c.971del ENSP00000453346.1:p.Gly324AlafsTer?
ENST00000558518.5:c.971del ENSP00000454071.1:p.Gly324AlafsTer?
ENST00000560467.1:c.541-832del
NM_000527.4:c.971del , LRG_274t1:c.971del NP_000518.1:p.Gly324AlafsTer?
NM_001195798.1:c.971del NP_001182727.1:p.Gly324AlafsTer?
NM_001195799.1:c.848del NP_001182728.1:p.Gly283AlafsTer?
NM_001195800.1:c.467del NP_001182729.1:p.Gly156AlafsTer?
NM_001195803.1:c.590del NP_001182732.1:p.Gly197AlafsTer?
XM_011528010.1:c.971del XP_011526312.1:p.Gly324AlafsTer?
XM_011528011.1:c.590del XP_011526313.1:p.Gly197AlafsTer?
XR_244074.2:n.1121del
XM_011528010.2:c.971del XP_011526312.1:p.Gly324AlafsTer?
XR_001753685.2:n.1088del
XR_001753686.2:n.1088del
NM_000527.5:c.971del MANE Select NP_000518.1:p.Gly324AlafsTer?
NM_001195798.2:c.971del NP_001182727.1:p.Gly324AlafsTer?
NM_001195799.2:c.848del NP_001182728.1:p.Gly283AlafsTer?
NM_001195800.2:c.467del NP_001182729.1:p.Gly156AlafsTer?
NM_001195803.2:c.590del NP_001182732.1:p.Gly197AlafsTer?