Canonical Allele Identifier: CA404080004
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 1034427
ClinVar RCV Id: RCV001337149
dbSNP Id: rs2077300275
MyVariant Identifiers: chr19:g.11217326C>A (hg19) chr19:g.11106650C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11106650C>A , CM000681.2:g.11106650C>A GRCh38
NC_000019.9:g.11217326C>A , CM000681.1:g.11217326C>A GRCh37
NC_000019.8:g.11078326C>A NCBI36
NG_009060.1:g.22270C>A , LRG_274:g.22270C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1038C>A ENSP00000252444.6:p.Asp346Glu
ENST00000559340.2:c.780C>A ENSP00000453696.2:p.Asp260Glu
ENST00000560467.2:c.780C>A ENSP00000453513.2:p.Asp260Glu
ENST00000558518.6:c.780C>A MANE Select ENSP00000454071.1:p.Asp260Glu
ENST00000252444.9:c.1034C>A
ENST00000455727.6:c.314-742C>A ENSP00000397829.2:n.314-742C>A
ENST00000535915.5:c.657C>A ENSP00000440520.1:p.Asp219Glu
ENST00000545707.5:c.399C>A ENSP00000437639.1:p.Asp133Glu
ENST00000557933.5:c.780C>A ENSP00000453557.1:p.Asp260Glu
ENST00000558013.5:c.780C>A ENSP00000453346.1:p.Asp260Glu
ENST00000558518.5:c.780C>A ENSP00000454071.1:p.Asp260Glu
ENST00000558528.1:n.295C>A
ENST00000560467.1:c.380C>A
NM_000527.4:c.780C>A , LRG_274t1:c.780C>A NP_000518.1:p.Asp260Glu
NM_001195798.1:c.780C>A NP_001182727.1:p.Asp260Glu
NM_001195799.1:c.657C>A NP_001182728.1:p.Asp219Glu
NM_001195800.1:c.314-742C>A NP_001182729.1:n.314-742C>A
NM_001195803.1:c.399C>A NP_001182732.1:p.Asp133Glu
XM_011528010.1:c.780C>A XP_011526312.1:p.Asp260Glu
XM_011528011.1:c.399C>A XP_011526313.1:p.Asp133Glu
XR_244074.2:n.930C>A
XM_011528010.2:c.780C>A XP_011526312.1:p.Asp260Glu
XR_001753685.2:n.897C>A
XR_001753686.2:n.897C>A
NM_000527.5:c.780C>A MANE Select NP_000518.1:p.Asp260Glu
NM_001195798.2:c.780C>A NP_001182727.1:p.Asp260Glu
NM_001195799.2:c.657C>A NP_001182728.1:p.Asp219Glu
NM_001195800.2:c.314-742C>A NP_001182729.1:n.314-742C>A
NM_001195803.2:c.399C>A NP_001182732.1:p.Asp133Glu
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