Canonical Allele Identifier: CA10585793
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 252242
ClinVar RCV Id: RCV000237516
dbSNP Id: rs879255150

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123183C>G , CM000681.2:g.11123183C>G GRCh38
NC_000019.9:g.11233859C>G , CM000681.1:g.11233859C>G GRCh37
NC_000019.8:g.11094859C>G NCBI36
NG_009060.1:g.38803C>G , LRG_274:g.38803C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.2408C>G ENSP00000252444.6:p.Ala803Gly
ENST00000559340.2:c.*219C>G ENSP00000453696.2:n.*219C>G
ENST00000560467.2:c.2030C>G ENSP00000453513.2:p.Ala677Gly
ENST00000558518.6:c.2150C>G MANE Select ENSP00000454071.1:p.Ala717Gly
ENST00000252444.9:c.2404C>G
ENST00000455727.6:c.1646C>G ENSP00000397829.2:p.Ala549Gly
ENST00000535915.5:c.2027C>G ENSP00000440520.1:p.Ala676Gly
ENST00000545707.5:c.1616C>G ENSP00000437639.1:p.Ala539Gly
ENST00000557933.5:c.2150C>G ENSP00000453557.1:p.Ala717Gly
ENST00000558013.5:c.2150C>G ENSP00000453346.1:p.Ala717Gly
ENST00000558518.5:c.2150C>G ENSP00000454071.1:p.Ala717Gly
NM_000527.4:c.2150C>G , LRG_274t1:c.2150C>G NP_000518.1:p.Ala717Gly
NM_001195798.1:c.2150C>G NP_001182727.1:p.Ala717Gly
NM_001195799.1:c.2027C>G NP_001182728.1:p.Ala676Gly
NM_001195800.1:c.1646C>G NP_001182729.1:p.Ala549Gly
NM_001195803.1:c.1616C>G NP_001182732.1:p.Ala539Gly
XM_011528010.1:c.2150C>G XP_011526312.1:p.Ala717Gly
XM_011528011.1:c.1769C>G XP_011526313.1:p.Ala590Gly
XR_244074.2:n.2160C>G
XM_011528010.2:c.2150C>G XP_011526312.1:p.Ala717Gly
XR_001753685.2:n.2484C>G
XR_001753686.2:n.2127C>G
NM_000527.5:c.2150C>G MANE Select NP_000518.1:p.Ala717Gly
NM_001195798.2:c.2150C>G NP_001182727.1:p.Ala717Gly
NM_001195799.2:c.2027C>G NP_001182728.1:p.Ala676Gly
NM_001195800.2:c.1646C>G NP_001182729.1:p.Ala549Gly
NM_001195803.2:c.1616C>G NP_001182732.1:p.Ala539Gly