Canonical Allele Identifier: CA2322767273
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105222_11105241delinsCCCAAGACGTGCTCCCAGGA , CM000681.2:g.11105222_11105241delinsCCCAAGACGTGCTCCCAGGA GRCh38
NC_000019.9:g.11215898_11215917delinsCCCAAGACGTGCTCCCAGGA , CM000681.1:g.11215898_11215917delinsCCCAAGACGTGCTCCCAGGA GRCh37
NC_000019.8:g.11076898_11076917delinsCCCAAGACGTGCTCCCAGGA NCBI36
NG_009060.1:g.20842_20861delinsCCCAAGACGTGCTCCCAGGA , LRG_274:g.20842_20861delinsCCCAAGACGTGCTCCCAGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.574_593delinsCCCAAGACGTGCTCCCAGGA ENSP00000252444.6:p.Pro192=
ENST00000559340.2:c.316_335delinsCCCAAGACGTGCTCCCAGGA ENSP00000453696.2:p.Pro106=
ENST00000560467.2:c.316_335delinsCCCAAGACGTGCTCCCAGGA ENSP00000453513.2:p.Pro106=
ENST00000558518.6:c.316_335delinsCCCAAGACGTGCTCCCAGGA MANE Select ENSP00000454071.1:p.Pro106=
ENST00000252444.9:c.570_589delinsCCCAAGACGTGCTCCCAGGA
ENST00000455727.6:c.314-2170_314-2151delinsCCCAAGACGTGCTCCCAGGA ENSP00000397829.2:n.314-2170_314-2151delinsCCCAAGACGTGCTCCCAG...
ENST00000535915.5:c.193_212delinsCCCAAGACGTGCTCCCAGGA ENSP00000440520.1:p.Pro65=
ENST00000545707.5:c.314-1343_314-1324delinsCCCAAGACGTGCTCCCAGGA ENSP00000437639.1:n.314-1343_314-1324delinsCCCAAGACGTGCTCCCAG...
ENST00000557933.5:c.316_335delinsCCCAAGACGTGCTCCCAGGA ENSP00000453557.1:p.Pro106=
ENST00000558013.5:c.316_335delinsCCCAAGACGTGCTCCCAGGA ENSP00000453346.1:p.Pro106=
ENST00000558518.5:c.316_335delinsCCCAAGACGTGCTCCCAGGA ENSP00000454071.1:p.Pro106=
NM_000527.4:c.316_335delinsCCCAAGACGTGCTCCCAGGA , LRG_274t1:c.316_335delinsCCCAAGACGTGCTCCCAGGA NP_000518.1:p.Pro106=
NM_001195798.1:c.316_335delinsCCCAAGACGTGCTCCCAGGA NP_001182727.1:p.Pro106=
NM_001195799.1:c.193_212delinsCCCAAGACGTGCTCCCAGGA NP_001182728.1:p.Pro65=
NM_001195800.1:c.314-2170_314-2151delinsCCCAAGACGTGCTCCCAGGA NP_001182729.1:n.314-2170_314-2151delinsCCCAAGACGTGCTCCCAGGA
NM_001195803.1:c.314-1343_314-1324delinsCCCAAGACGTGCTCCCAGGA NP_001182732.1:n.314-1343_314-1324delinsCCCAAGACGTGCTCCCAGGA
XM_011528010.1:c.316_335delinsCCCAAGACGTGCTCCCAGGA XP_011526312.1:p.Pro106=
XM_011528011.1:c.314-1343_314-1324delinsCCCAAGACGTGCTCCCAGGA XP_011526313.1:n.314-1343_314-1324delinsCCCAAGACGTGCTCCCAGGA
XR_244074.2:n.466_485delinsCCCAAGACGTGCTCCCAGGA
XM_011528010.2:c.316_335delinsCCCAAGACGTGCTCCCAGGA XP_011526312.1:p.Pro106=
XR_001753685.2:n.433_452delinsCCCAAGACGTGCTCCCAGGA
XR_001753686.2:n.433_452delinsCCCAAGACGTGCTCCCAGGA
NM_000527.5:c.316_335delinsCCCAAGACGTGCTCCCAGGA MANE Select NP_000518.1:p.Pro106=
NM_001195798.2:c.316_335delinsCCCAAGACGTGCTCCCAGGA NP_001182727.1:p.Pro106=
NM_001195799.2:c.193_212delinsCCCAAGACGTGCTCCCAGGA NP_001182728.1:p.Pro65=
NM_001195800.2:c.314-2170_314-2151delinsCCCAAGACGTGCTCCCAGGA NP_001182729.1:n.314-2170_314-2151delinsCCCAAGACGTGCTCCCAGGA
NM_001195803.2:c.314-1343_314-1324delinsCCCAAGACGTGCTCCCAGGA NP_001182732.1:n.314-1343_314-1324delinsCCCAAGACGTGCTCCCAGGA