Canonical Allele Identifier: CA2322775724
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120656_11120657delinsTG , CM000681.2:g.11120656_11120657delinsTG GRCh38
NC_000019.9:g.11231332_11231333delinsTG , CM000681.1:g.11231332_11231333delinsTG GRCh37
NC_000019.8:g.11092332_11092333delinsTG NCBI36
NG_009060.1:g.36276_36277delinsTG , LRG_274:g.36276_36277delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2398+134_2398+135delinsTG ENSP00000252444.6:n.2398+134_2398+135delinsTG
ENST00000559340.2:c.*209+134_*209+135delinsTG ENSP00000453696.2:n.*209+134_*209+135delinsTG
ENST00000560467.2:c.2020+134_2020+135delinsTG ENSP00000453513.2:n.2020+134_2020+135delinsTG
ENST00000558518.6:c.2140+134_2140+135delinsTG MANE Select ENSP00000454071.1:n.2140+134_2140+135delinsTG
ENST00000252444.9:c.2394+134_2394+135delinsTG
ENST00000455727.6:c.1636+134_1636+135delinsTG ENSP00000397829.2:n.1636+134_1636+135delinsTG
ENST00000535915.5:c.2017+134_2017+135delinsTG ENSP00000440520.1:n.2017+134_2017+135delinsTG
ENST00000545707.5:c.1606+423_1606+424delinsTG ENSP00000437639.1:n.1606+423_1606+424delinsTG
ENST00000557933.5:c.2140+134_2140+135delinsTG ENSP00000453557.1:n.2140+134_2140+135delinsTG
ENST00000558013.5:c.2140+134_2140+135delinsTG ENSP00000453346.1:n.2140+134_2140+135delinsTG
ENST00000558518.5:c.2140+134_2140+135delinsTG ENSP00000454071.1:n.2140+134_2140+135delinsTG
NM_000527.4:c.2140+134_2140+135delinsTG , LRG_274t1:c.2140+134_2140+135delinsTG NP_000518.1:n.2140+134_2140+135delinsTG
NM_001195798.1:c.2140+134_2140+135delinsTG NP_001182727.1:n.2140+134_2140+135delinsTG
NM_001195799.1:c.2017+134_2017+135delinsTG NP_001182728.1:n.2017+134_2017+135delinsTG
NM_001195800.1:c.1636+134_1636+135delinsTG NP_001182729.1:n.1636+134_1636+135delinsTG
NM_001195803.1:c.1606+423_1606+424delinsTG NP_001182732.1:n.1606+423_1606+424delinsTG
XM_011528010.1:c.2140+134_2140+135delinsTG XP_011526312.1:n.2140+134_2140+135delinsTG
XM_011528011.1:c.1759+134_1759+135delinsTG XP_011526313.1:n.1759+134_1759+135delinsTG
XR_244074.2:n.2150+134_2150+135delinsTG
XM_011528010.2:c.2140+134_2140+135delinsTG XP_011526312.1:n.2140+134_2140+135delinsTG
XR_001753685.2:n.2391_2392delinsTG
XR_001753686.2:n.2117+134_2117+135delinsTG
NM_000527.5:c.2140+134_2140+135delinsTG MANE Select NP_000518.1:n.2140+134_2140+135delinsTG
NM_001195798.2:c.2140+134_2140+135delinsTG NP_001182727.1:n.2140+134_2140+135delinsTG
NM_001195799.2:c.2017+134_2017+135delinsTG NP_001182728.1:n.2017+134_2017+135delinsTG
NM_001195800.2:c.1636+134_1636+135delinsTG NP_001182729.1:n.1636+134_1636+135delinsTG
NM_001195803.2:c.1606+423_1606+424delinsTG NP_001182732.1:n.1606+423_1606+424delinsTG