Canonical Allele Identifier: CA10584907
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251209
ClinVar RCV Id: RCV000237450
dbSNP Id: rs879254517

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105321G>A , CM000681.2:g.11105321G>A GRCh38
NC_000019.9:g.11215997G>A , CM000681.1:g.11215997G>A GRCh37
NC_000019.8:g.11076997G>A NCBI36
NG_009060.1:g.20941G>A , LRG_274:g.20941G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.673G>A ENSP00000252444.6:p.Asp225Asn
ENST00000559340.2:c.415G>A ENSP00000453696.2:p.Asp139Asn
ENST00000560467.2:c.415G>A ENSP00000453513.2:p.Asp139Asn
ENST00000558518.6:c.415G>A MANE Select ENSP00000454071.1:p.Asp139Asn
ENST00000252444.9:c.669G>A
ENST00000455727.6:c.314-2071G>A ENSP00000397829.2:n.314-2071G>A
ENST00000535915.5:c.292G>A ENSP00000440520.1:p.Asp98Asn
ENST00000545707.5:c.314-1244G>A ENSP00000437639.1:n.314-1244G>A
ENST00000557933.5:c.415G>A ENSP00000453557.1:p.Asp139Asn
ENST00000558013.5:c.415G>A ENSP00000453346.1:p.Asp139Asn
ENST00000558518.5:c.415G>A ENSP00000454071.1:p.Asp139Asn
ENST00000560467.1:c.15G>A
NM_000527.4:c.415G>A , LRG_274t1:c.415G>A NP_000518.1:p.Asp139Asn
NM_001195798.1:c.415G>A NP_001182727.1:p.Asp139Asn
NM_001195799.1:c.292G>A NP_001182728.1:p.Asp98Asn
NM_001195800.1:c.314-2071G>A NP_001182729.1:n.314-2071G>A
NM_001195803.1:c.314-1244G>A NP_001182732.1:n.314-1244G>A
XM_011528010.1:c.415G>A XP_011526312.1:p.Asp139Asn
XM_011528011.1:c.314-1244G>A XP_011526313.1:n.314-1244G>A
XR_244074.2:n.565G>A
XM_011528010.2:c.415G>A XP_011526312.1:p.Asp139Asn
XR_001753685.2:n.532G>A
XR_001753686.2:n.532G>A
NM_000527.5:c.415G>A MANE Select NP_000518.1:p.Asp139Asn
NM_001195798.2:c.415G>A NP_001182727.1:p.Asp139Asn
NM_001195799.2:c.292G>A NP_001182728.1:p.Asp98Asn
NM_001195800.2:c.314-2071G>A NP_001182729.1:n.314-2071G>A
NM_001195803.2:c.314-1244G>A NP_001182732.1:n.314-1244G>A