Canonical Allele Identifier: CA2322767602
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105571_11105594delinsGCAAGGACAAATCTGACGAGGAAA , CM000681.2:g.11105571_11105594delinsGCAAGGACAAATCTGACGAGGAAA GRCh38
NC_000019.9:g.11216247_11216270delinsGCAAGGACAAATCTGACGAGGAAA , CM000681.1:g.11216247_11216270delinsGCAAGGACAAATCTGACGAGGAAA GRCh37
NC_000019.8:g.11077247_11077270delinsGCAAGGACAAATCTGACGAGGAAA NCBI36
NG_009060.1:g.21191_21214delinsGCAAGGACAAATCTGACGAGGAAA , LRG_274:g.21191_21214delinsGCAAGGACAAATCTGACGAGGAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.923_946delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000252444.6:p.Cys308=
ENST00000559340.2:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000453696.2:p.Cys222=
ENST00000560467.2:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000453513.2:p.Cys222=
ENST00000558518.6:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA MANE Select ENSP00000454071.1:p.Cys222=
ENST00000252444.9:c.919_942delinsGCAAGGACAAATCTGACGAGGAAA
ENST00000455727.6:c.314-1821_314-1798delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000397829.2:n.314-1821_314-1798deli...
ENST00000535915.5:c.542_565delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000440520.1:p.Cys181=
ENST00000545707.5:c.314-994_314-971delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000437639.1:n.314-994_314-971delins...
ENST00000557933.5:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000453557.1:p.Cys222=
ENST00000558013.5:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000453346.1:p.Cys222=
ENST00000558518.5:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA ENSP00000454071.1:p.Cys222=
ENST00000560467.1:c.265_288delinsGCAAGGACAAATCTGACGAGGAAA
NM_000527.4:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA , LRG_274t1:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA NP_000518.1:p.Cys222=
NM_001195798.1:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA NP_001182727.1:p.Cys222=
NM_001195799.1:c.542_565delinsGCAAGGACAAATCTGACGAGGAAA NP_001182728.1:p.Cys181=
NM_001195800.1:c.314-1821_314-1798delinsGCAAGGACAAATCTGACGAGGAAA NP_001182729.1:n.314-1821_314-1798delinsG...
NM_001195803.1:c.314-994_314-971delinsGCAAGGACAAATCTGACGAGGAAA NP_001182732.1:n.314-994_314-971delinsGCA...
XM_011528010.1:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA XP_011526312.1:p.Cys222=
XM_011528011.1:c.314-994_314-971delinsGCAAGGACAAATCTGACGAGGAAA XP_011526313.1:n.314-994_314-971delinsGCA...
XR_244074.2:n.815_838delinsGCAAGGACAAATCTGACGAGGAAA
XM_011528010.2:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA XP_011526312.1:p.Cys222=
XR_001753685.2:n.782_805delinsGCAAGGACAAATCTGACGAGGAAA
XR_001753686.2:n.782_805delinsGCAAGGACAAATCTGACGAGGAAA
NM_000527.5:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA MANE Select NP_000518.1:p.Cys222=
NM_001195798.2:c.665_688delinsGCAAGGACAAATCTGACGAGGAAA NP_001182727.1:p.Cys222=
NM_001195799.2:c.542_565delinsGCAAGGACAAATCTGACGAGGAAA NP_001182728.1:p.Cys181=
NM_001195800.2:c.314-1821_314-1798delinsGCAAGGACAAATCTGACGAGGAAA NP_001182729.1:n.314-1821_314-1798delinsG...
NM_001195803.2:c.314-994_314-971delinsGCAAGGACAAATCTGACGAGGAAA NP_001182732.1:n.314-994_314-971delinsGCA...