Canonical Allele Identifier: CA645509276
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 440486
ClinVar RCV Id: RCV000508768
dbSNP Id: rs1555804717

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11111523del , CM000681.2:g.11111523del GRCh38
NC_000019.9:g.11222199del , CM000681.1:g.11222199del GRCh37
NC_000019.8:g.11083199del NCBI36
NG_009060.1:g.27143del , LRG_274:g.27143del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1328del ENSP00000252444.6:p.Glu443GlyfsTer13
ENST00000559340.2:c.1070del ENSP00000453696.2:p.Glu357GlyfsTer13
ENST00000560467.2:c.950del ENSP00000453513.2:p.Glu317GlyfsTer13
ENST00000558518.6:c.1070del MANE Select ENSP00000454071.1:p.Glu357GlyfsTer13
ENST00000252444.9:c.1324del
ENST00000455727.6:c.566del ENSP00000397829.2:p.Glu189GlyfsTer13
ENST00000535915.5:c.947del ENSP00000440520.1:p.Glu316GlyfsTer13
ENST00000545707.5:c.689del ENSP00000437639.1:p.Glu230GlyfsTer13
ENST00000557933.5:c.1070del ENSP00000453557.1:p.Glu357GlyfsTer13
ENST00000558013.5:c.1070del ENSP00000453346.1:p.Glu357GlyfsTer13
ENST00000558518.5:c.1070del ENSP00000454071.1:p.Glu357GlyfsTer13
ENST00000560173.1:n.69del
ENST00000560467.1:c.550del
NM_000527.4:c.1070del , LRG_274t1:c.1070del NP_000518.1:p.Glu357GlyfsTer13
NM_001195798.1:c.1070del NP_001182727.1:p.Glu357GlyfsTer13
NM_001195799.1:c.947del NP_001182728.1:p.Glu316GlyfsTer13
NM_001195800.1:c.566del NP_001182729.1:p.Glu189GlyfsTer13
NM_001195803.1:c.689del NP_001182732.1:p.Glu230GlyfsTer13
XM_011528010.1:c.1070del XP_011526312.1:p.Glu357GlyfsTer13
XM_011528011.1:c.689del XP_011526313.1:p.Glu230GlyfsTer13
XR_244074.2:n.1220del
XM_011528010.2:c.1070del XP_011526312.1:p.Glu357GlyfsTer13
XR_001753685.2:n.1187del
XR_001753686.2:n.1187del
NM_000527.5:c.1070del MANE Select NP_000518.1:p.Glu357GlyfsTer13
NM_001195798.2:c.1070del NP_001182727.1:p.Glu357GlyfsTer13
NM_001195799.2:c.947del NP_001182728.1:p.Glu316GlyfsTer13
NM_001195800.2:c.566del NP_001182729.1:p.Glu189GlyfsTer13
NM_001195803.2:c.689del NP_001182732.1:p.Glu230GlyfsTer13