Canonical Allele Identifier: CA2322767438
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105409_11105416delinsACAACGAC , CM000681.2:g.11105409_11105416delinsACAACGAC GRCh38
NC_000019.9:g.11216085_11216092delinsACAACGAC , CM000681.1:g.11216085_11216092delinsACAACGAC GRCh37
NC_000019.8:g.11077085_11077092delinsACAACGAC NCBI36
NG_009060.1:g.21029_21036delinsACAACGAC , LRG_274:g.21029_21036delinsACAACGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.761_768delinsACAACGAC ENSP00000252444.6:p.Asp254=
ENST00000559340.2:c.503_510delinsACAACGAC ENSP00000453696.2:p.Asp168=
ENST00000560467.2:c.503_510delinsACAACGAC ENSP00000453513.2:p.Asp168=
ENST00000558518.6:c.503_510delinsACAACGAC MANE Select ENSP00000454071.1:p.Asp168=
ENST00000252444.9:c.757_764delinsACAACGAC
ENST00000455727.6:c.314-1983_314-1976delinsACAACGAC ENSP00000397829.2:n.314-1983_314-1976delinsACAACGAC
ENST00000535915.5:c.380_387delinsACAACGAC ENSP00000440520.1:p.Asp127=
ENST00000545707.5:c.314-1156_314-1149delinsACAACGAC ENSP00000437639.1:n.314-1156_314-1149delinsACAACGAC
ENST00000557933.5:c.503_510delinsACAACGAC ENSP00000453557.1:p.Asp168=
ENST00000558013.5:c.503_510delinsACAACGAC ENSP00000453346.1:p.Asp168=
ENST00000558518.5:c.503_510delinsACAACGAC ENSP00000454071.1:p.Asp168=
ENST00000560467.1:c.103_110delinsACAACGAC
NM_000527.4:c.503_510delinsACAACGAC , LRG_274t1:c.503_510delinsACAACGAC NP_000518.1:p.Asp168=
NM_001195798.1:c.503_510delinsACAACGAC NP_001182727.1:p.Asp168=
NM_001195799.1:c.380_387delinsACAACGAC NP_001182728.1:p.Asp127=
NM_001195800.1:c.314-1983_314-1976delinsACAACGAC NP_001182729.1:n.314-1983_314-1976delinsACAACGAC
NM_001195803.1:c.314-1156_314-1149delinsACAACGAC NP_001182732.1:n.314-1156_314-1149delinsACAACGAC
XM_011528010.1:c.503_510delinsACAACGAC XP_011526312.1:p.Asp168=
XM_011528011.1:c.314-1156_314-1149delinsACAACGAC XP_011526313.1:n.314-1156_314-1149delinsACAACGAC
XR_244074.2:n.653_660delinsACAACGAC
XM_011528010.2:c.503_510delinsACAACGAC XP_011526312.1:p.Asp168=
XR_001753685.2:n.620_627delinsACAACGAC
XR_001753686.2:n.620_627delinsACAACGAC
NM_000527.5:c.503_510delinsACAACGAC MANE Select NP_000518.1:p.Asp168=
NM_001195798.2:c.503_510delinsACAACGAC NP_001182727.1:p.Asp168=
NM_001195799.2:c.380_387delinsACAACGAC NP_001182728.1:p.Asp127=
NM_001195800.2:c.314-1983_314-1976delinsACAACGAC NP_001182729.1:n.314-1983_314-1976delinsACAACGAC
NM_001195803.2:c.314-1156_314-1149delinsACAACGAC NP_001182732.1:n.314-1156_314-1149delinsACAACGAC