Canonical Allele Identifier: CA10584952
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251260
ClinVar RCV Id: RCV000237766 RCV001186870
dbSNP Id: rs879254549
MyVariant Identifiers: chr19:g.11216085A>G (hg19) chr19:g.11105409A>G (hg38)
PubMed: PMID:20145306
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105409A>G , CM000681.2:g.11105409A>G GRCh38
NC_000019.9:g.11216085A>G , CM000681.1:g.11216085A>G GRCh37
NC_000019.8:g.11077085A>G NCBI36
NG_009060.1:g.21029A>G , LRG_274:g.21029A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.761A>G ENSP00000252444.6:p.Asp254Gly
ENST00000559340.2:c.503A>G ENSP00000453696.2:p.Asp168Gly
ENST00000560467.2:c.503A>G ENSP00000453513.2:p.Asp168Gly
ENST00000558518.6:c.503A>G MANE Select ENSP00000454071.1:p.Asp168Gly
ENST00000252444.9:c.757A>G
ENST00000455727.6:c.314-1983A>G ENSP00000397829.2:n.314-1983A>G
ENST00000535915.5:c.380A>G ENSP00000440520.1:p.Asp127Gly
ENST00000545707.5:c.314-1156A>G ENSP00000437639.1:n.314-1156A>G
ENST00000557933.5:c.503A>G ENSP00000453557.1:p.Asp168Gly
ENST00000558013.5:c.503A>G ENSP00000453346.1:p.Asp168Gly
ENST00000558518.5:c.503A>G ENSP00000454071.1:p.Asp168Gly
ENST00000560467.1:c.103A>G
NM_000527.4:c.503A>G , LRG_274t1:c.503A>G NP_000518.1:p.Asp168Gly
NM_001195798.1:c.503A>G NP_001182727.1:p.Asp168Gly
NM_001195799.1:c.380A>G NP_001182728.1:p.Asp127Gly
NM_001195800.1:c.314-1983A>G NP_001182729.1:n.314-1983A>G
NM_001195803.1:c.314-1156A>G NP_001182732.1:n.314-1156A>G
XM_011528010.1:c.503A>G XP_011526312.1:p.Asp168Gly
XM_011528011.1:c.314-1156A>G XP_011526313.1:n.314-1156A>G
XR_244074.2:n.653A>G
XM_011528010.2:c.503A>G XP_011526312.1:p.Asp168Gly
XR_001753685.2:n.620A>G
XR_001753686.2:n.620A>G
NM_000527.5:c.503A>G MANE Select NP_000518.1:p.Asp168Gly
NM_001195798.2:c.503A>G NP_001182727.1:p.Asp168Gly
NM_001195799.2:c.380A>G NP_001182728.1:p.Asp127Gly
NM_001195800.2:c.314-1983A>G NP_001182729.1:n.314-1983A>G
NM_001195803.2:c.314-1156A>G NP_001182732.1:n.314-1156A>G
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