Canonical Allele Identifier: CA2322772199
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11114042_11114043delinsGT , CM000681.2:g.11114042_11114043delinsGT GRCh38
NC_000019.9:g.11224718_11224719delinsGT , CM000681.1:g.11224718_11224719delinsGT GRCh37
NC_000019.8:g.11085718_11085719delinsGT NCBI36
NG_009060.1:g.29662_29663delinsGT , LRG_274:g.29662_29663delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1844+280_1844+281delinsGT ENSP00000252444.6:n.1844+280_1844+281delinsGT
ENST00000559340.2:c.1586+280_1586+281delinsGT ENSP00000453696.2:n.1586+280_1586+281delinsGT
ENST00000560467.2:c.1466+280_1466+281delinsGT ENSP00000453513.2:n.1466+280_1466+281delinsGT
ENST00000558518.6:c.1586+280_1586+281delinsGT MANE Select ENSP00000454071.1:n.1586+280_1586+281delinsGT
ENST00000252444.9:c.1840+280_1840+281delinsGT
ENST00000455727.6:c.1082+280_1082+281delinsGT ENSP00000397829.2:n.1082+280_1082+281delinsGT
ENST00000535915.5:c.1463+280_1463+281delinsGT ENSP00000440520.1:n.1463+280_1463+281delinsGT
ENST00000545707.5:c.1205+280_1205+281delinsGT ENSP00000437639.1:n.1205+280_1205+281delinsGT
ENST00000557933.5:c.1586+280_1586+281delinsGT ENSP00000453557.1:n.1586+280_1586+281delinsGT
ENST00000558013.5:c.1586+280_1586+281delinsGT ENSP00000453346.1:n.1586+280_1586+281delinsGT
ENST00000558518.5:c.1586+280_1586+281delinsGT ENSP00000454071.1:n.1586+280_1586+281delinsGT
ENST00000559340.1:c.307+280_307+281delinsGT
NM_000527.4:c.1586+280_1586+281delinsGT , LRG_274t1:c.1586+280_1586+281delinsGT NP_000518.1:n.1586+280_1586+281delinsGT
NM_001195798.1:c.1586+280_1586+281delinsGT NP_001182727.1:n.1586+280_1586+281delinsGT
NM_001195799.1:c.1463+280_1463+281delinsGT NP_001182728.1:n.1463+280_1463+281delinsGT
NM_001195800.1:c.1082+280_1082+281delinsGT NP_001182729.1:n.1082+280_1082+281delinsGT
NM_001195803.1:c.1205+280_1205+281delinsGT NP_001182732.1:n.1205+280_1205+281delinsGT
XM_011528010.1:c.1586+280_1586+281delinsGT XP_011526312.1:n.1586+280_1586+281delinsGT
XM_011528011.1:c.1205+280_1205+281delinsGT XP_011526313.1:n.1205+280_1205+281delinsGT
XR_244074.2:n.1736+280_1736+281delinsGT
XM_011528010.2:c.1586+280_1586+281delinsGT XP_011526312.1:n.1586+280_1586+281delinsGT
XR_001753685.2:n.1703+280_1703+281delinsGT
XR_001753686.2:n.1703+280_1703+281delinsGT
NM_000527.5:c.1586+280_1586+281delinsGT MANE Select NP_000518.1:n.1586+280_1586+281delinsGT
NM_001195798.2:c.1586+280_1586+281delinsGT NP_001182727.1:n.1586+280_1586+281delinsGT
NM_001195799.2:c.1463+280_1463+281delinsGT NP_001182728.1:n.1463+280_1463+281delinsGT
NM_001195800.2:c.1082+280_1082+281delinsGT NP_001182729.1:n.1082+280_1082+281delinsGT
NM_001195803.2:c.1205+280_1205+281delinsGT NP_001182732.1:n.1205+280_1205+281delinsGT