Canonical Allele Identifier: CA2322767589
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105565_11105582delinsCCGACTGCAAGGACAAAT , CM000681.2:g.11105565_11105582delinsCCGACTGCAAGGACAAAT GRCh38
NC_000019.9:g.11216241_11216258delinsCCGACTGCAAGGACAAAT , CM000681.1:g.11216241_11216258delinsCCGACTGCAAGGACAAAT GRCh37
NC_000019.8:g.11077241_11077258delinsCCGACTGCAAGGACAAAT NCBI36
NG_009060.1:g.21185_21202delinsCCGACTGCAAGGACAAAT , LRG_274:g.21185_21202delinsCCGACTGCAAGGACAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.917_934delinsCCGACTGCAAGGACAAAT ENSP00000252444.6:p.Pro306=
ENST00000559340.2:c.659_676delinsCCGACTGCAAGGACAAAT ENSP00000453696.2:p.Pro220=
ENST00000560467.2:c.659_676delinsCCGACTGCAAGGACAAAT ENSP00000453513.2:p.Pro220=
ENST00000558518.6:c.659_676delinsCCGACTGCAAGGACAAAT MANE Select ENSP00000454071.1:p.Pro220=
ENST00000252444.9:c.913_930delinsCCGACTGCAAGGACAAAT
ENST00000455727.6:c.314-1827_314-1810delinsCCGACTGCAAGGACAAAT ENSP00000397829.2:n.314-1827_314-1810deli...
ENST00000535915.5:c.536_553delinsCCGACTGCAAGGACAAAT ENSP00000440520.1:p.Pro179=
ENST00000545707.5:c.314-1000_314-983delinsCCGACTGCAAGGACAAAT ENSP00000437639.1:n.314-1000_314-983delin...
ENST00000557933.5:c.659_676delinsCCGACTGCAAGGACAAAT ENSP00000453557.1:p.Pro220=
ENST00000558013.5:c.659_676delinsCCGACTGCAAGGACAAAT ENSP00000453346.1:p.Pro220=
ENST00000558518.5:c.659_676delinsCCGACTGCAAGGACAAAT ENSP00000454071.1:p.Pro220=
ENST00000560467.1:c.259_276delinsCCGACTGCAAGGACAAAT
NM_000527.4:c.659_676delinsCCGACTGCAAGGACAAAT , LRG_274t1:c.659_676delinsCCGACTGCAAGGACAAAT NP_000518.1:p.Pro220=
NM_001195798.1:c.659_676delinsCCGACTGCAAGGACAAAT NP_001182727.1:p.Pro220=
NM_001195799.1:c.536_553delinsCCGACTGCAAGGACAAAT NP_001182728.1:p.Pro179=
NM_001195800.1:c.314-1827_314-1810delinsCCGACTGCAAGGACAAAT NP_001182729.1:n.314-1827_314-1810delinsC...
NM_001195803.1:c.314-1000_314-983delinsCCGACTGCAAGGACAAAT NP_001182732.1:n.314-1000_314-983delinsCC...
XM_011528010.1:c.659_676delinsCCGACTGCAAGGACAAAT XP_011526312.1:p.Pro220=
XM_011528011.1:c.314-1000_314-983delinsCCGACTGCAAGGACAAAT XP_011526313.1:n.314-1000_314-983delinsCC...
XR_244074.2:n.809_826delinsCCGACTGCAAGGACAAAT
XM_011528010.2:c.659_676delinsCCGACTGCAAGGACAAAT XP_011526312.1:p.Pro220=
XR_001753685.2:n.776_793delinsCCGACTGCAAGGACAAAT
XR_001753686.2:n.776_793delinsCCGACTGCAAGGACAAAT
NM_000527.5:c.659_676delinsCCGACTGCAAGGACAAAT MANE Select NP_000518.1:p.Pro220=
NM_001195798.2:c.659_676delinsCCGACTGCAAGGACAAAT NP_001182727.1:p.Pro220=
NM_001195799.2:c.536_553delinsCCGACTGCAAGGACAAAT NP_001182728.1:p.Pro179=
NM_001195800.2:c.314-1827_314-1810delinsCCGACTGCAAGGACAAAT NP_001182729.1:n.314-1827_314-1810delinsC...
NM_001195803.2:c.314-1000_314-983delinsCCGACTGCAAGGACAAAT NP_001182732.1:n.314-1000_314-983delinsCC...