Canonical Allele Identifier: CA2582475763
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120657G>T , CM000681.2:g.11120657G>T GRCh38
NC_000019.9:g.11231333G>T , CM000681.1:g.11231333G>T GRCh37
NC_000019.8:g.11092333G>T NCBI36
NG_009060.1:g.36277G>T , LRG_274:g.36277G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2398+135G>T ENSP00000252444.6:n.2398+135G>T
ENST00000559340.2:c.*209+135G>T ENSP00000453696.2:n.*209+135G>T
ENST00000560467.2:c.2020+135G>T ENSP00000453513.2:n.2020+135G>T
ENST00000558518.6:c.2140+135G>T MANE Select ENSP00000454071.1:n.2140+135G>T
ENST00000252444.9:c.2394+135G>T
ENST00000455727.6:c.1636+135G>T ENSP00000397829.2:n.1636+135G>T
ENST00000535915.5:c.2017+135G>T ENSP00000440520.1:n.2017+135G>T
ENST00000545707.5:c.1606+424G>T ENSP00000437639.1:n.1606+424G>T
ENST00000557933.5:c.2140+135G>T ENSP00000453557.1:n.2140+135G>T
ENST00000558013.5:c.2140+135G>T ENSP00000453346.1:n.2140+135G>T
ENST00000558518.5:c.2140+135G>T ENSP00000454071.1:n.2140+135G>T
NM_000527.4:c.2140+135G>T , LRG_274t1:c.2140+135G>T NP_000518.1:n.2140+135G>T
NM_001195798.1:c.2140+135G>T NP_001182727.1:n.2140+135G>T
NM_001195799.1:c.2017+135G>T NP_001182728.1:n.2017+135G>T
NM_001195800.1:c.1636+135G>T NP_001182729.1:n.1636+135G>T
NM_001195803.1:c.1606+424G>T NP_001182732.1:n.1606+424G>T
XM_011528010.1:c.2140+135G>T XP_011526312.1:n.2140+135G>T
XM_011528011.1:c.1759+135G>T XP_011526313.1:n.1759+135G>T
XR_244074.2:n.2150+135G>T
XM_011528010.2:c.2140+135G>T XP_011526312.1:n.2140+135G>T
XR_001753685.2:n.2392G>T
XR_001753686.2:n.2117+135G>T
NM_000527.5:c.2140+135G>T MANE Select NP_000518.1:n.2140+135G>T
NM_001195798.2:c.2140+135G>T NP_001182727.1:n.2140+135G>T
NM_001195799.2:c.2017+135G>T NP_001182728.1:n.2017+135G>T
NM_001195800.2:c.1636+135G>T NP_001182729.1:n.1636+135G>T
NM_001195803.2:c.1606+424G>T NP_001182732.1:n.1606+424G>T