Canonical Allele Identifier: CA2582476259
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128070del , CM000681.2:g.11128070del GRCh38
NC_000019.9:g.11238746del , CM000681.1:g.11238746del GRCh37
NC_000019.8:g.11099746del NCBI36
NG_009060.1:g.43690del , LRG_274:g.43690del

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.2632del ENSP00000252444.6:p.Ile878LeufsTer?
ENST00000559340.2:c.*443del ENSP00000453696.2:n.*443del
ENST00000560467.2:c.2254del ENSP00000453513.2:p.Ile752LeufsTer?
ENST00000558518.6:c.2374del MANE Select ENSP00000454071.1:p.Ile792LeufsTer?
ENST00000252444.9:c.2628del
ENST00000455727.6:c.1870del ENSP00000397829.2:p.Ile624LeufsTer?
ENST00000535915.5:c.2251del ENSP00000440520.1:p.Ile751LeufsTer?
ENST00000545707.5:c.1840del ENSP00000437639.1:p.Ile614LeufsTer?
ENST00000557933.5:c.2374del ENSP00000453557.1:p.Ile792LeufsTer?
ENST00000558013.5:c.2374del ENSP00000453346.1:p.Ile792LeufsTer?
ENST00000558518.5:c.2374del ENSP00000454071.1:p.Ile792LeufsTer?
ENST00000560628.1:n.108+416del
NM_000527.4:c.2374del , LRG_274t1:c.2374del NP_000518.1:p.Ile792LeufsTer?
NM_001195798.1:c.2374del NP_001182727.1:p.Ile792LeufsTer?
NM_001195799.1:c.2251del NP_001182728.1:p.Ile751LeufsTer?
NM_001195800.1:c.1870del NP_001182729.1:p.Ile624LeufsTer?
NM_001195803.1:c.1840del NP_001182732.1:p.Ile614LeufsTer?
XM_011528010.1:c.2312-1443del XP_011526312.1:n.2312-1443del
XM_011528011.1:c.1993del XP_011526313.1:p.Ile665LeufsTer?
XR_244074.2:n.2384del
XM_011528010.2:c.2312-1443del XP_011526312.1:n.2312-1443del
XR_001753685.2:n.2708del
XR_001753686.2:n.2351del
NM_000527.5:c.2374del MANE Select NP_000518.1:p.Ile792LeufsTer?
NM_001195798.2:c.2374del NP_001182727.1:p.Ile792LeufsTer?
NM_001195799.2:c.2251del NP_001182728.1:p.Ile751LeufsTer?
NM_001195800.2:c.1870del NP_001182729.1:p.Ile624LeufsTer?
NM_001195803.2:c.1840del NP_001182732.1:p.Ile614LeufsTer?