Canonical Allele Identifier: CA2322775721
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120649_11120650delinsCT , CM000681.2:g.11120649_11120650delinsCT GRCh38
NC_000019.9:g.11231325_11231326delinsCT , CM000681.1:g.11231325_11231326delinsCT GRCh37
NC_000019.8:g.11092325_11092326delinsCT NCBI36
NG_009060.1:g.36269_36270delinsCT , LRG_274:g.36269_36270delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2398+127_2398+128delinsCT ENSP00000252444.6:n.2398+127_2398+128delinsCT
ENST00000559340.2:c.*209+127_*209+128delinsCT ENSP00000453696.2:n.*209+127_*209+128delinsCT
ENST00000560467.2:c.2020+127_2020+128delinsCT ENSP00000453513.2:n.2020+127_2020+128delinsCT
ENST00000558518.6:c.2140+127_2140+128delinsCT MANE Select ENSP00000454071.1:n.2140+127_2140+128delinsCT
ENST00000252444.9:c.2394+127_2394+128delinsCT
ENST00000455727.6:c.1636+127_1636+128delinsCT ENSP00000397829.2:n.1636+127_1636+128delinsCT
ENST00000535915.5:c.2017+127_2017+128delinsCT ENSP00000440520.1:n.2017+127_2017+128delinsCT
ENST00000545707.5:c.1606+416_1606+417delinsCT ENSP00000437639.1:n.1606+416_1606+417delinsCT
ENST00000557933.5:c.2140+127_2140+128delinsCT ENSP00000453557.1:n.2140+127_2140+128delinsCT
ENST00000558013.5:c.2140+127_2140+128delinsCT ENSP00000453346.1:n.2140+127_2140+128delinsCT
ENST00000558518.5:c.2140+127_2140+128delinsCT ENSP00000454071.1:n.2140+127_2140+128delinsCT
NM_000527.4:c.2140+127_2140+128delinsCT , LRG_274t1:c.2140+127_2140+128delinsCT NP_000518.1:n.2140+127_2140+128delinsCT
NM_001195798.1:c.2140+127_2140+128delinsCT NP_001182727.1:n.2140+127_2140+128delinsCT
NM_001195799.1:c.2017+127_2017+128delinsCT NP_001182728.1:n.2017+127_2017+128delinsCT
NM_001195800.1:c.1636+127_1636+128delinsCT NP_001182729.1:n.1636+127_1636+128delinsCT
NM_001195803.1:c.1606+416_1606+417delinsCT NP_001182732.1:n.1606+416_1606+417delinsCT
XM_011528010.1:c.2140+127_2140+128delinsCT XP_011526312.1:n.2140+127_2140+128delinsCT
XM_011528011.1:c.1759+127_1759+128delinsCT XP_011526313.1:n.1759+127_1759+128delinsCT
XR_244074.2:n.2150+127_2150+128delinsCT
XM_011528010.2:c.2140+127_2140+128delinsCT XP_011526312.1:n.2140+127_2140+128delinsCT
XR_001753685.2:n.2384_2385delinsCT
XR_001753686.2:n.2117+127_2117+128delinsCT
NM_000527.5:c.2140+127_2140+128delinsCT MANE Select NP_000518.1:n.2140+127_2140+128delinsCT
NM_001195798.2:c.2140+127_2140+128delinsCT NP_001182727.1:n.2140+127_2140+128delinsCT
NM_001195799.2:c.2017+127_2017+128delinsCT NP_001182728.1:n.2017+127_2017+128delinsCT
NM_001195800.2:c.1636+127_1636+128delinsCT NP_001182729.1:n.1636+127_1636+128delinsCT
NM_001195803.2:c.1606+416_1606+417delinsCT NP_001182732.1:n.1606+416_1606+417delinsCT