Canonical Allele Identifier: CA2322767191
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105096_11105099delinsACTG , CM000681.2:g.11105096_11105099delinsACTG GRCh38
NC_000019.9:g.11215772_11215775delinsACTG , CM000681.1:g.11215772_11215775delinsACTG GRCh37
NC_000019.8:g.11076772_11076775delinsACTG NCBI36
NG_009060.1:g.20716_20719delinsACTG , LRG_274:g.20716_20719delinsACTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.572-124_572-121delinsACTG ENSP00000252444.6:n.572-124_572-121delinsACTG
ENST00000559340.2:c.314-124_314-121delinsACTG ENSP00000453696.2:n.314-124_314-121delinsACTG
ENST00000560467.2:c.314-124_314-121delinsACTG ENSP00000453513.2:n.314-124_314-121delinsACTG
ENST00000558518.6:c.314-124_314-121delinsACTG MANE Select ENSP00000454071.1:n.314-124_314-121delinsACTG
ENST00000252444.9:c.568-124_568-121delinsACTG
ENST00000455727.6:c.314-2296_314-2293delinsACTG ENSP00000397829.2:n.314-2296_314-2293delinsACTG
ENST00000535915.5:c.191-124_191-121delinsACTG ENSP00000440520.1:n.191-124_191-121delinsACTG
ENST00000545707.5:c.314-1469_314-1466delinsACTG ENSP00000437639.1:n.314-1469_314-1466delinsACTG
ENST00000557933.5:c.314-124_314-121delinsACTG ENSP00000453557.1:n.314-124_314-121delinsACTG
ENST00000558013.5:c.314-124_314-121delinsACTG ENSP00000453346.1:n.314-124_314-121delinsACTG
ENST00000558518.5:c.314-124_314-121delinsACTG ENSP00000454071.1:n.314-124_314-121delinsACTG
NM_000527.4:c.314-124_314-121delinsACTG , LRG_274t1:c.314-124_314-121delinsACTG NP_000518.1:n.314-124_314-121delinsACTG
NM_001195798.1:c.314-124_314-121delinsACTG NP_001182727.1:n.314-124_314-121delinsACTG
NM_001195799.1:c.191-124_191-121delinsACTG NP_001182728.1:n.191-124_191-121delinsACTG
NM_001195800.1:c.314-2296_314-2293delinsACTG NP_001182729.1:n.314-2296_314-2293delinsACTG
NM_001195803.1:c.314-1469_314-1466delinsACTG NP_001182732.1:n.314-1469_314-1466delinsACTG
XM_011528010.1:c.314-124_314-121delinsACTG XP_011526312.1:n.314-124_314-121delinsACTG
XM_011528011.1:c.314-1469_314-1466delinsACTG XP_011526313.1:n.314-1469_314-1466delinsACTG
XR_244074.2:n.464-124_464-121delinsACTG
XM_011528010.2:c.314-124_314-121delinsACTG XP_011526312.1:n.314-124_314-121delinsACTG
XR_001753685.2:n.431-124_431-121delinsACTG
XR_001753686.2:n.431-124_431-121delinsACTG
NM_000527.5:c.314-124_314-121delinsACTG MANE Select NP_000518.1:n.314-124_314-121delinsACTG
NM_001195798.2:c.314-124_314-121delinsACTG NP_001182727.1:n.314-124_314-121delinsACTG
NM_001195799.2:c.191-124_191-121delinsACTG NP_001182728.1:n.191-124_191-121delinsACTG
NM_001195800.2:c.314-2296_314-2293delinsACTG NP_001182729.1:n.314-2296_314-2293delinsACTG
NM_001195803.2:c.314-1469_314-1466delinsACTG NP_001182732.1:n.314-1469_314-1466delinsACTG