Canonical Allele Identifier: CA2017997787
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 2138230
ClinVar RCV Id: RCV003041354

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120131_11120135delinsGATCATCAACC , CM000681.2:g.11120131_11120135delinsGATCATCAACC GRCh38
NC_000019.9:g.11230807_11230811delinsGATCATCAACC , CM000681.1:g.11230807_11230811delinsGATCATCAACC GRCh37
NC_000019.8:g.11091807_11091811delinsGATCATCAACC NCBI36
NG_009060.1:g.35751_35755delinsGATCATCAACC , LRG_274:g.35751_35755delinsGATCATCAACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2143_2147delinsGATCATCAACC ENSP00000252444.6:p.Phe715_Ser716delinsAspHisGlnPro
ENST00000559340.2:c.1745_1749delinsGATCATCAACC ENSP00000453696.2:p.Phe582Ter
ENST00000560467.2:c.1765_1769delinsGATCATCAACC ENSP00000453513.2:p.Phe589_Ser590delinsAspHisGlnPro
ENST00000558518.6:c.1885_1889delinsGATCATCAACC MANE Select ENSP00000454071.1:p.Phe629_Ser630delinsAspHisGlnPro
ENST00000252444.9:c.2139_2143delinsGATCATCAACC
ENST00000455727.6:c.1381_1385delinsGATCATCAACC ENSP00000397829.2:p.Phe461_Ser462delinsAspHisGlnPro
ENST00000535915.5:c.1762_1766delinsGATCATCAACC ENSP00000440520.1:p.Phe588_Ser589delinsAspHisGlnPro
ENST00000545707.5:c.1504_1508delinsGATCATCAACC ENSP00000437639.1:p.Phe502_Ser503delinsAspHisGlnPro
ENST00000557933.5:c.1885_1889delinsGATCATCAACC ENSP00000453557.1:p.Phe629_Ser630delinsAspHisGlnPro
ENST00000558013.5:c.1885_1889delinsGATCATCAACC ENSP00000453346.1:p.Phe629_Ser630delinsAspHisGlnPro
ENST00000558518.5:c.1885_1889delinsGATCATCAACC ENSP00000454071.1:p.Phe629_Ser630delinsAspHisGlnPro
ENST00000559340.1:c.466_470delinsGATCATCAACC
NM_000527.4:c.1885_1889delinsGATCATCAACC , LRG_274t1:c.1885_1889delinsGATCATCAACC NP_000518.1:p.Phe629_Ser630delinsAspHisGlnPro
NM_001195798.1:c.1885_1889delinsGATCATCAACC NP_001182727.1:p.Phe629_Ser630delinsAspHisGlnPro
NM_001195799.1:c.1762_1766delinsGATCATCAACC NP_001182728.1:p.Phe588_Ser589delinsAspHisGlnPro
NM_001195800.1:c.1381_1385delinsGATCATCAACC NP_001182729.1:p.Phe461_Ser462delinsAspHisGlnPro
NM_001195803.1:c.1504_1508delinsGATCATCAACC NP_001182732.1:p.Phe502_Ser503delinsAspHisGlnPro
XM_011528010.1:c.1885_1889delinsGATCATCAACC XP_011526312.1:p.Phe629_Ser630delinsAspHisGlnPro
XM_011528011.1:c.1504_1508delinsGATCATCAACC XP_011526313.1:p.Phe502_Ser503delinsAspHisGlnPro
XR_244074.2:n.1895_1899delinsGATCATCAACC
XM_011528010.2:c.1885_1889delinsGATCATCAACC XP_011526312.1:p.Phe629_Ser630delinsAspHisGlnPro
XR_001753685.2:n.2002_2006delinsGATCATCAACC
XR_001753686.2:n.1862_1866delinsGATCATCAACC
NM_000527.5:c.1885_1889delinsGATCATCAACC MANE Select NP_000518.1:p.Phe629_Ser630delinsAspHisGlnPro
NM_001195798.2:c.1885_1889delinsGATCATCAACC NP_001182727.1:p.Phe629_Ser630delinsAspHisGlnPro
NM_001195799.2:c.1762_1766delinsGATCATCAACC NP_001182728.1:p.Phe588_Ser589delinsAspHisGlnPro
NM_001195800.2:c.1381_1385delinsGATCATCAACC NP_001182729.1:p.Phe461_Ser462delinsAspHisGlnPro
NM_001195803.2:c.1504_1508delinsGATCATCAACC NP_001182732.1:p.Phe502_Ser503delinsAspHisGlnPro