Canonical Allele Identifier: CA2322774205
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11117926_11117928delinsCTG , CM000681.2:g.11117926_11117928delinsCTG GRCh38
NC_000019.9:g.11228602_11228604delinsCTG , CM000681.1:g.11228602_11228604delinsCTG GRCh37
NC_000019.8:g.11089602_11089604delinsCTG NCBI36
NG_009060.1:g.33546_33548delinsCTG , LRG_274:g.33546_33548delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2103+928_2103+930delinsCTG ENSP00000252444.6:n.2103+928_2103+930delinsCTG
ENST00000559340.2:c.1705+1714_1705+1716delinsCTG ENSP00000453696.2:n.1705+1714_1705+1716delinsCTG
ENST00000560467.2:c.1725+928_1725+930delinsCTG ENSP00000453513.2:n.1725+928_1725+930delinsCTG
ENST00000558518.6:c.1845+928_1845+930delinsCTG MANE Select ENSP00000454071.1:n.1845+928_1845+930delinsCTG
ENST00000252444.9:c.2099+928_2099+930delinsCTG
ENST00000455727.6:c.1341+928_1341+930delinsCTG ENSP00000397829.2:n.1341+928_1341+930delinsCTG
ENST00000535915.5:c.1722+928_1722+930delinsCTG ENSP00000440520.1:n.1722+928_1722+930delinsCTG
ENST00000545707.5:c.1464+928_1464+930delinsCTG ENSP00000437639.1:n.1464+928_1464+930delinsCTG
ENST00000557933.5:c.1845+928_1845+930delinsCTG ENSP00000453557.1:n.1845+928_1845+930delinsCTG
ENST00000558013.5:c.1845+928_1845+930delinsCTG ENSP00000453346.1:n.1845+928_1845+930delinsCTG
ENST00000558518.5:c.1845+928_1845+930delinsCTG ENSP00000454071.1:n.1845+928_1845+930delinsCTG
ENST00000559340.1:c.426+1714_426+1716delinsCTG
NM_000527.4:c.1845+928_1845+930delinsCTG , LRG_274t1:c.1845+928_1845+930delinsCTG NP_000518.1:n.1845+928_1845+930delinsCTG
NM_001195798.1:c.1845+928_1845+930delinsCTG NP_001182727.1:n.1845+928_1845+930delinsCTG
NM_001195799.1:c.1722+928_1722+930delinsCTG NP_001182728.1:n.1722+928_1722+930delinsCTG
NM_001195800.1:c.1341+928_1341+930delinsCTG NP_001182729.1:n.1341+928_1341+930delinsCTG
NM_001195803.1:c.1464+928_1464+930delinsCTG NP_001182732.1:n.1464+928_1464+930delinsCTG
XM_011528010.1:c.1845+928_1845+930delinsCTG XP_011526312.1:n.1845+928_1845+930delinsCTG
XM_011528011.1:c.1464+928_1464+930delinsCTG XP_011526313.1:n.1464+928_1464+930delinsCTG
XR_244074.2:n.1855+1714_1855+1716delinsCTG
XM_011528010.2:c.1845+928_1845+930delinsCTG XP_011526312.1:n.1845+928_1845+930delinsCTG
XR_001753685.2:n.1962+928_1962+930delinsCTG
XR_001753686.2:n.1822+1714_1822+1716delinsCTG
NM_000527.5:c.1845+928_1845+930delinsCTG MANE Select NP_000518.1:n.1845+928_1845+930delinsCTG
NM_001195798.2:c.1845+928_1845+930delinsCTG NP_001182727.1:n.1845+928_1845+930delinsCTG
NM_001195799.2:c.1722+928_1722+930delinsCTG NP_001182728.1:n.1722+928_1722+930delinsCTG
NM_001195800.2:c.1341+928_1341+930delinsCTG NP_001182729.1:n.1341+928_1341+930delinsCTG
NM_001195803.2:c.1464+928_1464+930delinsCTG NP_001182732.1:n.1464+928_1464+930delinsCTG