Canonical Allele Identifier: CA2322780127
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129293_11129294delinsGT , CM000681.2:g.11129293_11129294delinsGT GRCh38
NC_000019.9:g.11239969_11239970delinsGT , CM000681.1:g.11239969_11239970delinsGT GRCh37
NC_000019.8:g.11100969_11100970delinsGT NCBI36
NG_009060.1:g.44913_44914delinsGT , LRG_274:g.44913_44914delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2648-220_2648-219delinsGT ENSP00000252444.6:n.2648-220_2648-219delinsGT
ENST00000559340.2:c.*459-220_*459-219delinsGT ENSP00000453696.2:n.*459-220_*459-219delinsGT
ENST00000560467.2:c.2270-220_2270-219delinsGT ENSP00000453513.2:n.2270-220_2270-219delinsGT
ENST00000558518.6:c.2390-220_2390-219delinsGT MANE Select ENSP00000454071.1:n.2390-220_2390-219delinsGT
ENST00000252444.9:c.2644-220_2644-219delinsGT
ENST00000455727.6:c.1886-220_1886-219delinsGT ENSP00000397829.2:n.1886-220_1886-219delinsGT
ENST00000535915.5:c.2267-220_2267-219delinsGT ENSP00000440520.1:n.2267-220_2267-219delinsGT
ENST00000545707.5:c.1856-220_1856-219delinsGT ENSP00000437639.1:n.1856-220_1856-219delinsGT
ENST00000557933.5:c.2390-158_2390-157delinsGT ENSP00000453557.1:n.2390-158_2390-157delinsGT
ENST00000558013.5:c.2390-220_2390-219delinsGT ENSP00000453346.1:n.2390-220_2390-219delinsGT
ENST00000558518.5:c.2390-220_2390-219delinsGT ENSP00000454071.1:n.2390-220_2390-219delinsGT
ENST00000560628.1:n.108+1639_108+1640delinsGT
NM_000527.4:c.2390-220_2390-219delinsGT , LRG_274t1:c.2390-220_2390-219delinsGT NP_000518.1:n.2390-220_2390-219delinsGT
NM_001195798.1:c.2390-220_2390-219delinsGT NP_001182727.1:n.2390-220_2390-219delinsGT
NM_001195799.1:c.2267-220_2267-219delinsGT NP_001182728.1:n.2267-220_2267-219delinsGT
NM_001195800.1:c.1886-220_1886-219delinsGT NP_001182729.1:n.1886-220_1886-219delinsGT
NM_001195803.1:c.1856-220_1856-219delinsGT NP_001182732.1:n.1856-220_1856-219delinsGT
XM_011528010.1:c.2312-220_2312-219delinsGT XP_011526312.1:n.2312-220_2312-219delinsGT
XM_011528011.1:c.2009-220_2009-219delinsGT XP_011526313.1:n.2009-220_2009-219delinsGT
XR_244074.2:n.2400-220_2400-219delinsGT
XM_011528010.2:c.2312-220_2312-219delinsGT XP_011526312.1:n.2312-220_2312-219delinsGT
XR_001753685.2:n.2724-220_2724-219delinsGT
XR_001753686.2:n.2367-220_2367-219delinsGT
NM_000527.5:c.2390-220_2390-219delinsGT MANE Select NP_000518.1:n.2390-220_2390-219delinsGT
NM_001195798.2:c.2390-220_2390-219delinsGT NP_001182727.1:n.2390-220_2390-219delinsGT
NM_001195799.2:c.2267-220_2267-219delinsGT NP_001182728.1:n.2267-220_2267-219delinsGT
NM_001195800.2:c.1886-220_1886-219delinsGT NP_001182729.1:n.1886-220_1886-219delinsGT
NM_001195803.2:c.1856-220_1856-219delinsGT NP_001182732.1:n.1856-220_1856-219delinsGT