Canonical Allele Identifier: CA10585622
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 252041
ClinVar RCV Id: RCV000237963
dbSNP Id: rs879255028

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116955dup , CM000681.2:g.11116955dup GRCh38
NC_000019.9:g.11227631dup , CM000681.1:g.11227631dup GRCh37
NC_000019.8:g.11088631dup NCBI36
NG_009060.1:g.32575dup , LRG_274:g.32575dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2060dup ENSP00000252444.6:p.Asp687GlufsTer2
ENST00000559340.2:c.1705+743dup ENSP00000453696.2:n.1705+743dup
ENST00000560467.2:c.1682dup ENSP00000453513.2:p.Asp561GlufsTer2
ENST00000558518.6:c.1802dup MANE Select ENSP00000454071.1:p.Asp601GlufsTer2
ENST00000252444.9:c.2056dup
ENST00000455727.6:c.1298dup ENSP00000397829.2:p.Asp433GlufsTer2
ENST00000535915.5:c.1679dup ENSP00000440520.1:p.Asp560GlufsTer2
ENST00000545707.5:c.1421dup ENSP00000437639.1:p.Asp474GlufsTer2
ENST00000557933.5:c.1802dup ENSP00000453557.1:p.Asp601GlufsTer2
ENST00000558013.5:c.1802dup ENSP00000453346.1:p.Asp601GlufsTer2
ENST00000558518.5:c.1802dup ENSP00000454071.1:p.Asp601GlufsTer2
ENST00000559340.1:c.426+743dup
NM_000527.4:c.1802dup , LRG_274t1:c.1802dup NP_000518.1:p.Asp601GlufsTer2
NM_001195798.1:c.1802dup NP_001182727.1:p.Asp601GlufsTer2
NM_001195799.1:c.1679dup NP_001182728.1:p.Asp560GlufsTer2
NM_001195800.1:c.1298dup NP_001182729.1:p.Asp433GlufsTer2
NM_001195803.1:c.1421dup NP_001182732.1:p.Asp474GlufsTer2
XM_011528010.1:c.1802dup XP_011526312.1:p.Asp601GlufsTer2
XM_011528011.1:c.1421dup XP_011526313.1:p.Asp474GlufsTer2
XR_244074.2:n.1855+743dup
XM_011528010.2:c.1802dup XP_011526312.1:p.Asp601GlufsTer2
XR_001753685.2:n.1919dup
XR_001753686.2:n.1822+743dup
NM_000527.5:c.1802dup MANE Select NP_000518.1:p.Asp601GlufsTer2
NM_001195798.2:c.1802dup NP_001182727.1:p.Asp601GlufsTer2
NM_001195799.2:c.1679dup NP_001182728.1:p.Asp560GlufsTer2
NM_001195800.2:c.1298dup NP_001182729.1:p.Asp433GlufsTer2
NM_001195803.2:c.1421dup NP_001182732.1:p.Asp474GlufsTer2