Canonical Allele Identifier: CA2322767175
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs2077263648

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105063_11105064insGGCAGTGCCTGTGGTTC , CM000681.2:g.11105063_11105064insGGCAGTGCCTGTGGTTC GRCh38
NC_000019.9:g.11215739_11215740insGGCAGTGCCTGTGGTTC , CM000681.1:g.11215739_11215740insGGCAGTGCCTGTGGTTC GRCh37
NC_000019.8:g.11076739_11076740insGGCAGTGCCTGTGGTTC NCBI36
NG_009060.1:g.20683_20684insGGCAGTGCCTGTGGTTC , LRG_274:g.20683_20684insGGCAGTGCCTGTGGTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.572-157_572-156insGGCAGTGCCTGTGGTTC ENSP00000252444.6:n.572-157_572-156insGGCAGTGCCTGTGGTTC
ENST00000559340.2:c.314-157_314-156insGGCAGTGCCTGTGGTTC ENSP00000453696.2:n.314-157_314-156insGGCAGTGCCTGTGGTTC
ENST00000560467.2:c.314-157_314-156insGGCAGTGCCTGTGGTTC ENSP00000453513.2:n.314-157_314-156insGGCAGTGCCTGTGGTTC
ENST00000558518.6:c.314-157_314-156insGGCAGTGCCTGTGGTTC MANE Select ENSP00000454071.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
ENST00000252444.9:c.568-157_568-156insGGCAGTGCCTGTGGTTC
ENST00000455727.6:c.313+2277_313+2278insGGCAGTGCCTGTGGTTC ENSP00000397829.2:n.313+2277_313+2278insGGCAGTGCCTGTGGTTC
ENST00000535915.5:c.191-157_191-156insGGCAGTGCCTGTGGTTC ENSP00000440520.1:n.191-157_191-156insGGCAGTGCCTGTGGTTC
ENST00000545707.5:c.314-1502_314-1501insGGCAGTGCCTGTGGTTC ENSP00000437639.1:n.314-1502_314-1501insGGCAGTGCCTGTGGTTC
ENST00000557933.5:c.314-157_314-156insGGCAGTGCCTGTGGTTC ENSP00000453557.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
ENST00000558013.5:c.314-157_314-156insGGCAGTGCCTGTGGTTC ENSP00000453346.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
ENST00000558518.5:c.314-157_314-156insGGCAGTGCCTGTGGTTC ENSP00000454071.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
NM_000527.4:c.314-157_314-156insGGCAGTGCCTGTGGTTC , LRG_274t1:c.314-157_314-156insGGCAGTGCCTGTGGTTC NP_000518.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
NM_001195798.1:c.314-157_314-156insGGCAGTGCCTGTGGTTC NP_001182727.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
NM_001195799.1:c.191-157_191-156insGGCAGTGCCTGTGGTTC NP_001182728.1:n.191-157_191-156insGGCAGTGCCTGTGGTTC
NM_001195800.1:c.313+2277_313+2278insGGCAGTGCCTGTGGTTC NP_001182729.1:n.313+2277_313+2278insGGCAGTGCCTGTGGTTC
NM_001195803.1:c.314-1502_314-1501insGGCAGTGCCTGTGGTTC NP_001182732.1:n.314-1502_314-1501insGGCAGTGCCTGTGGTTC
XM_011528010.1:c.314-157_314-156insGGCAGTGCCTGTGGTTC XP_011526312.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
XM_011528011.1:c.314-1502_314-1501insGGCAGTGCCTGTGGTTC XP_011526313.1:n.314-1502_314-1501insGGCAGTGCCTGTGGTTC
XR_244074.2:n.464-157_464-156insGGCAGTGCCTGTGGTTC
XM_011528010.2:c.314-157_314-156insGGCAGTGCCTGTGGTTC XP_011526312.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
XR_001753685.2:n.431-157_431-156insGGCAGTGCCTGTGGTTC
XR_001753686.2:n.431-157_431-156insGGCAGTGCCTGTGGTTC
NM_000527.5:c.314-157_314-156insGGCAGTGCCTGTGGTTC MANE Select NP_000518.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
NM_001195798.2:c.314-157_314-156insGGCAGTGCCTGTGGTTC NP_001182727.1:n.314-157_314-156insGGCAGTGCCTGTGGTTC
NM_001195799.2:c.191-157_191-156insGGCAGTGCCTGTGGTTC NP_001182728.1:n.191-157_191-156insGGCAGTGCCTGTGGTTC
NM_001195800.2:c.313+2277_313+2278insGGCAGTGCCTGTGGTTC NP_001182729.1:n.313+2277_313+2278insGGCAGTGCCTGTGGTTC
NM_001195803.2:c.314-1502_314-1501insGGCAGTGCCTGTGGTTC NP_001182732.1:n.314-1502_314-1501insGGCAGTGCCTGTGGTTC