Canonical Allele Identifier: CA2322767582
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105560_11105566delinsTGGCCCC , CM000681.2:g.11105560_11105566delinsTGGCCCC GRCh38
NC_000019.9:g.11216236_11216242delinsTGGCCCC , CM000681.1:g.11216236_11216242delinsTGGCCCC GRCh37
NC_000019.8:g.11077236_11077242delinsTGGCCCC NCBI36
NG_009060.1:g.21180_21186delinsTGGCCCC , LRG_274:g.21180_21186delinsTGGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.912_918delinsTGGCCCC ENSP00000252444.6:p.Gly304=
ENST00000559340.2:c.654_660delinsTGGCCCC ENSP00000453696.2:p.Gly218=
ENST00000560467.2:c.654_660delinsTGGCCCC ENSP00000453513.2:p.Gly218=
ENST00000558518.6:c.654_660delinsTGGCCCC MANE Select ENSP00000454071.1:p.Gly218=
ENST00000252444.9:c.908_914delinsTGGCCCC
ENST00000455727.6:c.314-1832_314-1826delinsTGGCCCC ENSP00000397829.2:n.314-1832_314-1826delinsTGGCCCC
ENST00000535915.5:c.531_537delinsTGGCCCC ENSP00000440520.1:p.Gly177=
ENST00000545707.5:c.314-1005_314-999delinsTGGCCCC ENSP00000437639.1:n.314-1005_314-999delinsTGGCCCC
ENST00000557933.5:c.654_660delinsTGGCCCC ENSP00000453557.1:p.Gly218=
ENST00000558013.5:c.654_660delinsTGGCCCC ENSP00000453346.1:p.Gly218=
ENST00000558518.5:c.654_660delinsTGGCCCC ENSP00000454071.1:p.Gly218=
ENST00000560467.1:c.254_260delinsTGGCCCC
NM_000527.4:c.654_660delinsTGGCCCC , LRG_274t1:c.654_660delinsTGGCCCC NP_000518.1:p.Gly218=
NM_001195798.1:c.654_660delinsTGGCCCC NP_001182727.1:p.Gly218=
NM_001195799.1:c.531_537delinsTGGCCCC NP_001182728.1:p.Gly177=
NM_001195800.1:c.314-1832_314-1826delinsTGGCCCC NP_001182729.1:n.314-1832_314-1826delinsTGGCCCC
NM_001195803.1:c.314-1005_314-999delinsTGGCCCC NP_001182732.1:n.314-1005_314-999delinsTGGCCCC
XM_011528010.1:c.654_660delinsTGGCCCC XP_011526312.1:p.Gly218=
XM_011528011.1:c.314-1005_314-999delinsTGGCCCC XP_011526313.1:n.314-1005_314-999delinsTGGCCCC
XR_244074.2:n.804_810delinsTGGCCCC
XM_011528010.2:c.654_660delinsTGGCCCC XP_011526312.1:p.Gly218=
XR_001753685.2:n.771_777delinsTGGCCCC
XR_001753686.2:n.771_777delinsTGGCCCC
NM_000527.5:c.654_660delinsTGGCCCC MANE Select NP_000518.1:p.Gly218=
NM_001195798.2:c.654_660delinsTGGCCCC NP_001182727.1:p.Gly218=
NM_001195799.2:c.531_537delinsTGGCCCC NP_001182728.1:p.Gly177=
NM_001195800.2:c.314-1832_314-1826delinsTGGCCCC NP_001182729.1:n.314-1832_314-1826delinsTGGCCCC
NM_001195803.2:c.314-1005_314-999delinsTGGCCCC NP_001182732.1:n.314-1005_314-999delinsTGGCCCC