Canonical Allele Identifier: CA2322770212
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110652_11110701delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT , CM000681.2:g.11110652_11110701delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT GRCh38
NC_000019.9:g.11221328_11221377delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT , CM000681.1:g.11221328_11221377delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT GRCh37
NC_000019.8:g.11082328_11082377delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NCBI36
NG_009060.1:g.26272_26321delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT , LRG_274:g.26272_26321delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1199_1248delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000252444.6:p.Gly400=
ENST00000559340.2:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000453696.2:p.Gly314=
ENST00000560467.2:c.941-862_941-813delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000453513.2:n.941-862_941-813delinsGGACCAACGAATGCTTGGAC...
ENST00000558518.6:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT MANE Select ENSP00000454071.1:p.Gly314=
ENST00000252444.9:c.1195_1244delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT
ENST00000455727.6:c.437_486delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000397829.2:p.Gly146=
ENST00000535915.5:c.818_867delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000440520.1:p.Gly273=
ENST00000545707.5:c.560_609delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000437639.1:p.Gly187=
ENST00000557933.5:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000453557.1:p.Gly314=
ENST00000558013.5:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000453346.1:p.Gly314=
ENST00000558518.5:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT ENSP00000454071.1:p.Gly314=
ENST00000560467.1:c.541-862_541-813delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT
NM_000527.4:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT , LRG_274t1:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_000518.1:p.Gly314=
NM_001195798.1:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182727.1:p.Gly314=
NM_001195799.1:c.818_867delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182728.1:p.Gly273=
NM_001195800.1:c.437_486delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182729.1:p.Gly146=
NM_001195803.1:c.560_609delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182732.1:p.Gly187=
XM_011528010.1:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT XP_011526312.1:p.Gly314=
XM_011528011.1:c.560_609delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT XP_011526313.1:p.Gly187=
XR_244074.2:n.1091_1140delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT
XM_011528010.2:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT XP_011526312.1:p.Gly314=
XR_001753685.2:n.1058_1107delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT
XR_001753686.2:n.1058_1107delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT
NM_000527.5:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT MANE Select NP_000518.1:p.Gly314=
NM_001195798.2:c.941_990delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182727.1:p.Gly314=
NM_001195799.2:c.818_867delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182728.1:p.Gly273=
NM_001195800.2:c.437_486delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182729.1:p.Gly146=
NM_001195803.2:c.560_609delinsGGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT NP_001182732.1:p.Gly187=