Canonical Allele Identifier: CA10585225
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251570
dbSNP Id: rs879254738

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110663T>C , CM000681.2:g.11110663T>C GRCh38
NC_000019.9:g.11221339T>C , CM000681.1:g.11221339T>C GRCh37
NC_000019.8:g.11082339T>C NCBI36
NG_009060.1:g.26283T>C , LRG_274:g.26283T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1210T>C ENSP00000252444.6:p.Cys404Arg
ENST00000559340.2:c.952T>C ENSP00000453696.2:p.Cys318Arg
ENST00000560467.2:c.941-851T>C ENSP00000453513.2:n.941-851T>C
ENST00000558518.6:c.952T>C MANE Select ENSP00000454071.1:p.Cys318Arg
ENST00000252444.9:c.1206T>C
ENST00000455727.6:c.448T>C ENSP00000397829.2:p.Cys150Arg
ENST00000535915.5:c.829T>C ENSP00000440520.1:p.Cys277Arg
ENST00000545707.5:c.571T>C ENSP00000437639.1:p.Cys191Arg
ENST00000557933.5:c.952T>C ENSP00000453557.1:p.Cys318Arg
ENST00000558013.5:c.952T>C ENSP00000453346.1:p.Cys318Arg
ENST00000558518.5:c.952T>C ENSP00000454071.1:p.Cys318Arg
ENST00000560467.1:c.541-851T>C
NM_000527.4:c.952T>C , LRG_274t1:c.952T>C NP_000518.1:p.Cys318Arg
NM_001195798.1:c.952T>C NP_001182727.1:p.Cys318Arg
NM_001195799.1:c.829T>C NP_001182728.1:p.Cys277Arg
NM_001195800.1:c.448T>C NP_001182729.1:p.Cys150Arg
NM_001195803.1:c.571T>C NP_001182732.1:p.Cys191Arg
XM_011528010.1:c.952T>C XP_011526312.1:p.Cys318Arg
XM_011528011.1:c.571T>C XP_011526313.1:p.Cys191Arg
XR_244074.2:n.1102T>C
XM_011528010.2:c.952T>C XP_011526312.1:p.Cys318Arg
XR_001753685.2:n.1069T>C
XR_001753686.2:n.1069T>C
NM_000527.5:c.952T>C MANE Select NP_000518.1:p.Cys318Arg
NM_001195798.2:c.952T>C NP_001182727.1:p.Cys318Arg
NM_001195799.2:c.829T>C NP_001182728.1:p.Cys277Arg
NM_001195800.2:c.448T>C NP_001182729.1:p.Cys150Arg
NM_001195803.2:c.571T>C NP_001182732.1:p.Cys191Arg