Canonical Allele Identifier: CA10585243
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251590
ClinVar RCV Id: RCV000238513 RCV000808601
dbSNP Id: rs879254751
MyVariant Identifiers: chr19:g.11221395del (hg19) chr19:g.11110719del (hg38)
PubMed: PMID:20809525
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110719del , CM000681.2:g.11110719del GRCh38
NC_000019.9:g.11221395del , CM000681.1:g.11221395del GRCh37
NC_000019.8:g.11082395del NCBI36
NG_009060.1:g.26339del , LRG_274:g.26339del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1266del ENSP00000252444.6:p.Tyr422Ter
ENST00000559340.2:c.1008del ENSP00000453696.2:p.Tyr336Ter
ENST00000560467.2:c.941-795del ENSP00000453513.2:n.941-795del
ENST00000558518.6:c.1008del MANE Select ENSP00000454071.1:p.Tyr336Ter
ENST00000252444.9:c.1262del
ENST00000455727.6:c.504del ENSP00000397829.2:p.Tyr168Ter
ENST00000535915.5:c.885del ENSP00000440520.1:p.Tyr295Ter
ENST00000545707.5:c.627del ENSP00000437639.1:p.Tyr209Ter
ENST00000557933.5:c.1008del ENSP00000453557.1:p.Tyr336Ter
ENST00000558013.5:c.1008del ENSP00000453346.1:p.Tyr336Ter
ENST00000558518.5:c.1008del ENSP00000454071.1:p.Tyr336Ter
ENST00000560173.1:n.7del
ENST00000560467.1:c.541-795del
NM_000527.4:c.1008del , LRG_274t1:c.1008del NP_000518.1:p.Tyr336Ter
NM_001195798.1:c.1008del NP_001182727.1:p.Tyr336Ter
NM_001195799.1:c.885del NP_001182728.1:p.Tyr295Ter
NM_001195800.1:c.504del NP_001182729.1:p.Tyr168Ter
NM_001195803.1:c.627del NP_001182732.1:p.Tyr209Ter
XM_011528010.1:c.1008del XP_011526312.1:p.Tyr336Ter
XM_011528011.1:c.627del XP_011526313.1:p.Tyr209Ter
XR_244074.2:n.1158del
XM_011528010.2:c.1008del XP_011526312.1:p.Tyr336Ter
XR_001753685.2:n.1125del
XR_001753686.2:n.1125del
NM_000527.5:c.1008del MANE Select NP_000518.1:p.Tyr336Ter
NM_001195798.2:c.1008del NP_001182727.1:p.Tyr336Ter
NM_001195799.2:c.885del NP_001182728.1:p.Tyr295Ter
NM_001195800.2:c.504del NP_001182729.1:p.Tyr168Ter
NM_001195803.2:c.627del NP_001182732.1:p.Tyr209Ter
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