Canonical Allele Identifier: CA404098203
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 1094170
ClinVar RCV Id: RCV001414605
dbSNP Id: rs752846235

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129514G>T , CM000681.2:g.11129514G>T GRCh38
NC_000019.9:g.11240190G>T , CM000681.1:g.11240190G>T GRCh37
NC_000019.8:g.11101190G>T NCBI36
NG_009060.1:g.45134G>T , LRG_274:g.45134G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2649G>T ENSP00000252444.6:p.Val883=
ENST00000559340.2:c.*460G>T ENSP00000453696.2:n.*460G>T
ENST00000560467.2:c.2271G>T ENSP00000453513.2:p.Val757=
ENST00000558518.6:c.2391G>T MANE Select ENSP00000454071.1:p.Val797=
ENST00000252444.9:c.2645G>T
ENST00000455727.6:c.1887G>T ENSP00000397829.2:p.Val629=
ENST00000535915.5:c.2268G>T ENSP00000440520.1:p.Val756=
ENST00000545707.5:c.1857G>T ENSP00000437639.1:p.Val619=
ENST00000557933.5:c.2453G>T ENSP00000453557.1:p.Cys818Phe
ENST00000558013.5:c.2391G>T ENSP00000453346.1:p.Val797=
ENST00000558518.5:c.2391G>T ENSP00000454071.1:p.Val797=
ENST00000560628.1:n.108+1860G>T
NM_000527.4:c.2391G>T , LRG_274t1:c.2391G>T NP_000518.1:p.Val797=
NM_001195798.1:c.2391G>T NP_001182727.1:p.Val797=
NM_001195799.1:c.2268G>T NP_001182728.1:p.Val756=
NM_001195800.1:c.1887G>T NP_001182729.1:p.Val629=
NM_001195803.1:c.1857G>T NP_001182732.1:p.Val619=
XM_011528010.1:c.2313G>T XP_011526312.1:p.Val771=
XM_011528011.1:c.2010G>T XP_011526313.1:p.Val670=
XR_244074.2:n.2401G>T
XM_011528010.2:c.2313G>T XP_011526312.1:p.Val771=
XR_001753685.2:n.2725G>T
XR_001753686.2:n.2368G>T
NM_000527.5:c.2391G>T MANE Select NP_000518.1:p.Val797=
NM_001195798.2:c.2391G>T NP_001182727.1:p.Val797=
NM_001195799.2:c.2268G>T NP_001182728.1:p.Val756=
NM_001195800.2:c.1887G>T NP_001182729.1:p.Val629=
NM_001195803.2:c.1857G>T NP_001182732.1:p.Val619=