Canonical Allele Identifier: CA2322768189
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11106640_11106641delinsGG , CM000681.2:g.11106640_11106641delinsGG GRCh38
NC_000019.9:g.11217316_11217317delinsGG , CM000681.1:g.11217316_11217317delinsGG GRCh37
NC_000019.8:g.11078316_11078317delinsGG NCBI36
NG_009060.1:g.22260_22261delinsGG , LRG_274:g.22260_22261delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1028_1029delinsGG ENSP00000252444.6:p.Arg343=
ENST00000559340.2:c.770_771delinsGG ENSP00000453696.2:p.Arg257=
ENST00000560467.2:c.770_771delinsGG ENSP00000453513.2:p.Arg257=
ENST00000558518.6:c.770_771delinsGG MANE Select ENSP00000454071.1:p.Arg257=
ENST00000252444.9:c.1024_1025delinsGG
ENST00000455727.6:c.314-752_314-751delinsGG ENSP00000397829.2:n.314-752_314-751delinsGG
ENST00000535915.5:c.647_648delinsGG ENSP00000440520.1:p.Arg216=
ENST00000545707.5:c.389_390delinsGG ENSP00000437639.1:p.Arg130=
ENST00000557933.5:c.770_771delinsGG ENSP00000453557.1:p.Arg257=
ENST00000558013.5:c.770_771delinsGG ENSP00000453346.1:p.Arg257=
ENST00000558518.5:c.770_771delinsGG ENSP00000454071.1:p.Arg257=
ENST00000558528.1:n.285_286delinsGG
ENST00000560467.1:c.370_371delinsGG
NM_000527.4:c.770_771delinsGG , LRG_274t1:c.770_771delinsGG NP_000518.1:p.Arg257=
NM_001195798.1:c.770_771delinsGG NP_001182727.1:p.Arg257=
NM_001195799.1:c.647_648delinsGG NP_001182728.1:p.Arg216=
NM_001195800.1:c.314-752_314-751delinsGG NP_001182729.1:n.314-752_314-751delinsGG
NM_001195803.1:c.389_390delinsGG NP_001182732.1:p.Arg130=
XM_011528010.1:c.770_771delinsGG XP_011526312.1:p.Arg257=
XM_011528011.1:c.389_390delinsGG XP_011526313.1:p.Arg130=
XR_244074.2:n.920_921delinsGG
XM_011528010.2:c.770_771delinsGG XP_011526312.1:p.Arg257=
XR_001753685.2:n.887_888delinsGG
XR_001753686.2:n.887_888delinsGG
NM_000527.5:c.770_771delinsGG MANE Select NP_000518.1:p.Arg257=
NM_001195798.2:c.770_771delinsGG NP_001182727.1:p.Arg257=
NM_001195799.2:c.647_648delinsGG NP_001182728.1:p.Arg216=
NM_001195800.2:c.314-752_314-751delinsGG NP_001182729.1:n.314-752_314-751delinsGG
NM_001195803.2:c.389_390delinsGG NP_001182732.1:p.Arg130=