Canonical Allele Identifier: CA2322767595
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105567_11105594delinsGACTGCAAGGACAAATCTGACGAGGAAA , CM000681.2:g.11105567_11105594delinsGACTGCAAGGACAAATCTGACGAGGAAA GRCh38
NC_000019.9:g.11216243_11216270delinsGACTGCAAGGACAAATCTGACGAGGAAA , CM000681.1:g.11216243_11216270delinsGACTGCAAGGACAAATCTGACGAGGAAA GRCh37
NC_000019.8:g.11077243_11077270delinsGACTGCAAGGACAAATCTGACGAGGAAA NCBI36
NG_009060.1:g.21187_21214delinsGACTGCAAGGACAAATCTGACGAGGAAA , LRG_274:g.21187_21214delinsGACTGCAAGGACAAATCTGACGAGGAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.919_946delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000252444.6:p.Asp307=
ENST00000559340.2:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000453696.2:p.Asp221=
ENST00000560467.2:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000453513.2:p.Asp221=
ENST00000558518.6:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA MANE Select ENSP00000454071.1:p.Asp221=
ENST00000252444.9:c.915_942delinsGACTGCAAGGACAAATCTGACGAGGAAA
ENST00000455727.6:c.314-1825_314-1798delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000397829.2:n.314-1825_314-1798deli...
ENST00000535915.5:c.538_565delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000440520.1:p.Asp180=
ENST00000545707.5:c.314-998_314-971delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000437639.1:n.314-998_314-971delins...
ENST00000557933.5:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000453557.1:p.Asp221=
ENST00000558013.5:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000453346.1:p.Asp221=
ENST00000558518.5:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA ENSP00000454071.1:p.Asp221=
ENST00000560467.1:c.261_288delinsGACTGCAAGGACAAATCTGACGAGGAAA
NM_000527.4:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA , LRG_274t1:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_000518.1:p.Asp221=
NM_001195798.1:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182727.1:p.Asp221=
NM_001195799.1:c.538_565delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182728.1:p.Asp180=
NM_001195800.1:c.314-1825_314-1798delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182729.1:n.314-1825_314-1798delinsG...
NM_001195803.1:c.314-998_314-971delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182732.1:n.314-998_314-971delinsGAC...
XM_011528010.1:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA XP_011526312.1:p.Asp221=
XM_011528011.1:c.314-998_314-971delinsGACTGCAAGGACAAATCTGACGAGGAAA XP_011526313.1:n.314-998_314-971delinsGAC...
XR_244074.2:n.811_838delinsGACTGCAAGGACAAATCTGACGAGGAAA
XM_011528010.2:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA XP_011526312.1:p.Asp221=
XR_001753685.2:n.778_805delinsGACTGCAAGGACAAATCTGACGAGGAAA
XR_001753686.2:n.778_805delinsGACTGCAAGGACAAATCTGACGAGGAAA
NM_000527.5:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA MANE Select NP_000518.1:p.Asp221=
NM_001195798.2:c.661_688delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182727.1:p.Asp221=
NM_001195799.2:c.538_565delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182728.1:p.Asp180=
NM_001195800.2:c.314-1825_314-1798delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182729.1:n.314-1825_314-1798delinsG...
NM_001195803.2:c.314-998_314-971delinsGACTGCAAGGACAAATCTGACGAGGAAA NP_001182732.1:n.314-998_314-971delinsGAC...