Canonical Allele Identifier: CA023561
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 183123
dbSNP Id: rs185098634

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116873C>T , CM000681.2:g.11116873C>T GRCh38
NC_000019.9:g.11227549C>T , CM000681.1:g.11227549C>T GRCh37
NC_000019.8:g.11088549C>T NCBI36
NG_009060.1:g.32493C>T , LRG_274:g.32493C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1978C>T ENSP00000252444.6:p.Arg660Cys
ENST00000559340.2:c.1705+661C>T ENSP00000453696.2:n.1705+661C>T
ENST00000560467.2:c.1600C>T ENSP00000453513.2:p.Arg534Cys
ENST00000558518.6:c.1720C>T MANE Select ENSP00000454071.1:p.Arg574Cys
ENST00000252444.9:c.1974C>T
ENST00000455727.6:c.1216C>T ENSP00000397829.2:p.Arg406Cys
ENST00000535915.5:c.1597C>T ENSP00000440520.1:p.Arg533Cys
ENST00000545707.5:c.1339C>T ENSP00000437639.1:p.Arg447Cys
ENST00000557933.5:c.1720C>T ENSP00000453557.1:p.Arg574Cys
ENST00000558013.5:c.1720C>T ENSP00000453346.1:p.Arg574Cys
ENST00000558518.5:c.1720C>T ENSP00000454071.1:p.Arg574Cys
ENST00000559340.1:c.426+661C>T
NM_000527.4:c.1720C>T , LRG_274t1:c.1720C>T NP_000518.1:p.Arg574Cys
NM_001195798.1:c.1720C>T NP_001182727.1:p.Arg574Cys
NM_001195799.1:c.1597C>T NP_001182728.1:p.Arg533Cys
NM_001195800.1:c.1216C>T NP_001182729.1:p.Arg406Cys
NM_001195803.1:c.1339C>T NP_001182732.1:p.Arg447Cys
XM_011528010.1:c.1720C>T XP_011526312.1:p.Arg574Cys
XM_011528011.1:c.1339C>T XP_011526313.1:p.Arg447Cys
XR_244074.2:n.1855+661C>T
XM_011528010.2:c.1720C>T XP_011526312.1:p.Arg574Cys
XR_001753685.2:n.1837C>T
XR_001753686.2:n.1822+661C>T
NM_000527.5:c.1720C>T MANE Select NP_000518.1:p.Arg574Cys
NM_001195798.2:c.1720C>T NP_001182727.1:p.Arg574Cys
NM_001195799.2:c.1597C>T NP_001182728.1:p.Arg533Cys
NM_001195800.2:c.1216C>T NP_001182729.1:p.Arg406Cys
NM_001195803.2:c.1339C>T NP_001182732.1:p.Arg447Cys