Canonical Allele Identifier: CA10585805
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 252254
ClinVar RCV Id: RCV000238564
dbSNP Id: rs879255162

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123231C>T , CM000681.2:g.11123231C>T GRCh38
NC_000019.9:g.11233907C>T , CM000681.1:g.11233907C>T GRCh37
NC_000019.8:g.11094907C>T NCBI36
NG_009060.1:g.38851C>T , LRG_274:g.38851C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2456C>T ENSP00000252444.6:p.Ser819Phe
ENST00000559340.2:c.*267C>T ENSP00000453696.2:n.*267C>T
ENST00000560467.2:c.2078C>T ENSP00000453513.2:p.Ser693Phe
ENST00000558518.6:c.2198C>T MANE Select ENSP00000454071.1:p.Ser733Phe
ENST00000252444.9:c.2452C>T
ENST00000455727.6:c.1694C>T ENSP00000397829.2:p.Ser565Phe
ENST00000535915.5:c.2075C>T ENSP00000440520.1:p.Ser692Phe
ENST00000545707.5:c.1664C>T ENSP00000437639.1:p.Ser555Phe
ENST00000557933.5:c.2198C>T ENSP00000453557.1:p.Ser733Phe
ENST00000558013.5:c.2198C>T ENSP00000453346.1:p.Ser733Phe
ENST00000558518.5:c.2198C>T ENSP00000454071.1:p.Ser733Phe
NM_000527.4:c.2198C>T , LRG_274t1:c.2198C>T NP_000518.1:p.Ser733Phe
NM_001195798.1:c.2198C>T NP_001182727.1:p.Ser733Phe
NM_001195799.1:c.2075C>T NP_001182728.1:p.Ser692Phe
NM_001195800.1:c.1694C>T NP_001182729.1:p.Ser565Phe
NM_001195803.1:c.1664C>T NP_001182732.1:p.Ser555Phe
XM_011528010.1:c.2198C>T XP_011526312.1:p.Ser733Phe
XM_011528011.1:c.1817C>T XP_011526313.1:p.Ser606Phe
XR_244074.2:n.2208C>T
XM_011528010.2:c.2198C>T XP_011526312.1:p.Ser733Phe
XR_001753685.2:n.2532C>T
XR_001753686.2:n.2175C>T
NM_000527.5:c.2198C>T MANE Select NP_000518.1:p.Ser733Phe
NM_001195798.2:c.2198C>T NP_001182727.1:p.Ser733Phe
NM_001195799.2:c.2075C>T NP_001182728.1:p.Ser692Phe
NM_001195800.2:c.1694C>T NP_001182729.1:p.Ser565Phe
NM_001195803.2:c.1664C>T NP_001182732.1:p.Ser555Phe