Canonical Allele Identifier: CA043633
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251234
dbSNP Id: rs763233960

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105357G>C , CM000681.2:g.11105357G>C GRCh38
NC_000019.9:g.11216033G>C , CM000681.1:g.11216033G>C GRCh37
NC_000019.8:g.11077033G>C NCBI36
NG_009060.1:g.20977G>C , LRG_274:g.20977G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.709G>C ENSP00000252444.6:p.Ala237Pro
ENST00000559340.2:c.451G>C ENSP00000453696.2:p.Ala151Pro
ENST00000560467.2:c.451G>C ENSP00000453513.2:p.Ala151Pro
ENST00000558518.6:c.451G>C MANE Select ENSP00000454071.1:p.Ala151Pro
ENST00000252444.9:c.705G>C
ENST00000455727.6:c.314-2035G>C ENSP00000397829.2:n.314-2035G>C
ENST00000535915.5:c.328G>C ENSP00000440520.1:p.Ala110Pro
ENST00000545707.5:c.314-1208G>C ENSP00000437639.1:n.314-1208G>C
ENST00000557933.5:c.451G>C ENSP00000453557.1:p.Ala151Pro
ENST00000558013.5:c.451G>C ENSP00000453346.1:p.Ala151Pro
ENST00000558518.5:c.451G>C ENSP00000454071.1:p.Ala151Pro
ENST00000560467.1:c.51G>C
NM_000527.4:c.451G>C , LRG_274t1:c.451G>C NP_000518.1:p.Ala151Pro
NM_001195798.1:c.451G>C NP_001182727.1:p.Ala151Pro
NM_001195799.1:c.328G>C NP_001182728.1:p.Ala110Pro
NM_001195800.1:c.314-2035G>C NP_001182729.1:n.314-2035G>C
NM_001195803.1:c.314-1208G>C NP_001182732.1:n.314-1208G>C
XM_011528010.1:c.451G>C XP_011526312.1:p.Ala151Pro
XM_011528011.1:c.314-1208G>C XP_011526313.1:n.314-1208G>C
XR_244074.2:n.601G>C
XM_011528010.2:c.451G>C XP_011526312.1:p.Ala151Pro
XR_001753685.2:n.568G>C
XR_001753686.2:n.568G>C
NM_000527.5:c.451G>C MANE Select NP_000518.1:p.Ala151Pro
NM_001195798.2:c.451G>C NP_001182727.1:p.Ala151Pro
NM_001195799.2:c.328G>C NP_001182728.1:p.Ala110Pro
NM_001195800.2:c.314-2035G>C NP_001182729.1:n.314-2035G>C
NM_001195803.2:c.314-1208G>C NP_001182732.1:n.314-1208G>C