Canonical Allele Identifier: CA993532450
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 955172
dbSNP Id: rs2077276693

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105487del , CM000681.2:g.11105487del GRCh38
NC_000019.9:g.11216163del , CM000681.1:g.11216163del GRCh37
NC_000019.8:g.11077163del NCBI36
NG_009060.1:g.21107del , LRG_274:g.21107del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.839del ENSP00000252444.6:p.Ser280IlefsTer12
ENST00000559340.2:c.581del ENSP00000453696.2:p.Ser194IlefsTer12
ENST00000560467.2:c.581del ENSP00000453513.2:p.Ser194IlefsTer12
ENST00000558518.6:c.581del MANE Select ENSP00000454071.1:p.Ser194IlefsTer12
ENST00000252444.9:c.835del
ENST00000455727.6:c.314-1905del ENSP00000397829.2:n.314-1905del
ENST00000535915.5:c.458del ENSP00000440520.1:p.Ser153IlefsTer12
ENST00000545707.5:c.314-1078del ENSP00000437639.1:n.314-1078del
ENST00000557933.5:c.581del ENSP00000453557.1:p.Ser194IlefsTer12
ENST00000558013.5:c.581del ENSP00000453346.1:p.Ser194IlefsTer12
ENST00000558518.5:c.581del ENSP00000454071.1:p.Ser194IlefsTer12
ENST00000560467.1:c.181del
NM_000527.4:c.581del , LRG_274t1:c.581del NP_000518.1:p.Ser194IlefsTer12
NM_001195798.1:c.581del NP_001182727.1:p.Ser194IlefsTer12
NM_001195799.1:c.458del NP_001182728.1:p.Ser153IlefsTer12
NM_001195800.1:c.314-1905del NP_001182729.1:n.314-1905del
NM_001195803.1:c.314-1078del NP_001182732.1:n.314-1078del
XM_011528010.1:c.581del XP_011526312.1:p.Ser194IlefsTer12
XM_011528011.1:c.314-1078del XP_011526313.1:n.314-1078del
XR_244074.2:n.731del
XM_011528010.2:c.581del XP_011526312.1:p.Ser194IlefsTer12
XR_001753685.2:n.698del
XR_001753686.2:n.698del
NM_000527.5:c.581del MANE Select NP_000518.1:p.Ser194IlefsTer12
NM_001195798.2:c.581del NP_001182727.1:p.Ser194IlefsTer12
NM_001195799.2:c.458del NP_001182728.1:p.Ser153IlefsTer12
NM_001195800.2:c.314-1905del NP_001182729.1:n.314-1905del
NM_001195803.2:c.314-1078del NP_001182732.1:n.314-1078del