Canonical Allele Identifier: CA2322780408
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129806_11129807delinsGC , CM000681.2:g.11129806_11129807delinsGC GRCh38
NC_000019.9:g.11240482_11240483delinsGC , CM000681.1:g.11240482_11240483delinsGC GRCh37
NC_000019.8:g.11101482_11101483delinsGC NCBI36
NG_009060.1:g.45426_45427delinsGC , LRG_274:g.45426_45427delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2805+136_2805+137delinsGC ENSP00000252444.6:n.2805+136_2805+137delinsGC
ENST00000559340.2:c.*616+136_*616+137delinsGC ENSP00000453696.2:n.*616+136_*616+137delinsGC
ENST00000560467.2:c.2427+136_2427+137delinsGC ENSP00000453513.2:n.2427+136_2427+137delinsGC
ENST00000558518.6:c.2547+136_2547+137delinsGC MANE Select ENSP00000454071.1:n.2547+136_2547+137delinsGC
ENST00000252444.9:c.2801+136_2801+137delinsGC
ENST00000455727.6:c.2043+136_2043+137delinsGC ENSP00000397829.2:n.2043+136_2043+137delinsGC
ENST00000535915.5:c.2424+136_2424+137delinsGC ENSP00000440520.1:n.2424+136_2424+137delinsGC
ENST00000545707.5:c.2013+136_2013+137delinsGC ENSP00000437639.1:n.2013+136_2013+137delinsGC
ENST00000557933.5:c.2609+136_2609+137delinsGC ENSP00000453557.1:n.2609+136_2609+137delinsGC
ENST00000558013.5:c.2547+136_2547+137delinsGC ENSP00000453346.1:n.2547+136_2547+137delinsGC
ENST00000558518.5:c.2547+136_2547+137delinsGC ENSP00000454071.1:n.2547+136_2547+137delinsGC
ENST00000560628.1:n.108+2152_108+2153delinsGC
NM_000527.4:c.2547+136_2547+137delinsGC , LRG_274t1:c.2547+136_2547+137delinsGC NP_000518.1:n.2547+136_2547+137delinsGC
NM_001195798.1:c.2547+136_2547+137delinsGC NP_001182727.1:n.2547+136_2547+137delinsGC
NM_001195799.1:c.2424+136_2424+137delinsGC NP_001182728.1:n.2424+136_2424+137delinsGC
NM_001195800.1:c.2043+136_2043+137delinsGC NP_001182729.1:n.2043+136_2043+137delinsGC
NM_001195803.1:c.2013+136_2013+137delinsGC NP_001182732.1:n.2013+136_2013+137delinsGC
XM_011528010.1:c.2469+136_2469+137delinsGC XP_011526312.1:n.2469+136_2469+137delinsGC
XM_011528011.1:c.2166+136_2166+137delinsGC XP_011526313.1:n.2166+136_2166+137delinsGC
XM_011528010.2:c.2469+136_2469+137delinsGC XP_011526312.1:n.2469+136_2469+137delinsGC
XR_001753685.2:n.2881+136_2881+137delinsGC
XR_001753686.2:n.2524+136_2524+137delinsGC
NM_000527.5:c.2547+136_2547+137delinsGC MANE Select NP_000518.1:n.2547+136_2547+137delinsGC
NM_001195798.2:c.2547+136_2547+137delinsGC NP_001182727.1:n.2547+136_2547+137delinsGC
NM_001195799.2:c.2424+136_2424+137delinsGC NP_001182728.1:n.2424+136_2424+137delinsGC
NM_001195800.2:c.2043+136_2043+137delinsGC NP_001182729.1:n.2043+136_2043+137delinsGC
NM_001195803.2:c.2013+136_2013+137delinsGC NP_001182732.1:n.2013+136_2013+137delinsGC