Canonical Allele Identifier: CA10584738
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 250988
dbSNP Id: rs6511720

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11091630G>T , CM000681.2:g.11091630G>T GRCh38
NC_000019.9:g.11202306G>T , CM000681.1:g.11202306G>T GRCh37
NC_000019.8:g.11063306G>T NCBI36
NG_009060.1:g.7250G>T , LRG_274:g.7250G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.325+711G>T ENSP00000252444.6:n.325+711G>T
ENST00000559340.2:c.67+2015G>T ENSP00000453696.2:n.67+2015G>T
ENST00000560467.2:c.67+2015G>T ENSP00000453513.2:n.67+2015G>T
ENST00000558518.6:c.67+2015G>T MANE Select ENSP00000454071.1:n.67+2015G>T
ENST00000252444.9:c.321+711G>T
ENST00000455727.6:c.67+2015G>T ENSP00000397829.2:n.67+2015G>T
ENST00000535915.5:c.67+2015G>T ENSP00000440520.1:n.67+2015G>T
ENST00000545707.5:c.67+2015G>T ENSP00000437639.1:n.67+2015G>T
ENST00000557933.5:c.67+2015G>T ENSP00000453557.1:n.67+2015G>T
ENST00000557958.1:n.153+2015G>T
ENST00000558013.5:c.67+2015G>T ENSP00000453346.1:n.67+2015G>T
ENST00000558518.5:c.67+2015G>T ENSP00000454071.1:n.67+2015G>T
ENST00000560502.5:n.153+2015G>T
NM_000527.4:c.67+2015G>T , LRG_274t1:c.67+2015G>T NP_000518.1:n.67+2015G>T
NM_001195798.1:c.67+2015G>T NP_001182727.1:n.67+2015G>T
NM_001195799.1:c.67+2015G>T NP_001182728.1:n.67+2015G>T
NM_001195800.1:c.67+2015G>T NP_001182729.1:n.67+2015G>T
NM_001195803.1:c.67+2015G>T NP_001182732.1:n.67+2015G>T
XM_011528010.1:c.67+2015G>T XP_011526312.1:n.67+2015G>T
XM_011528011.1:c.67+2015G>T XP_011526313.1:n.67+2015G>T
XR_244074.2:n.217+2015G>T
XM_011528010.2:c.67+2015G>T XP_011526312.1:n.67+2015G>T
XR_001753685.2:n.184+2015G>T
XR_001753686.2:n.184+2015G>T
NM_000527.5:c.67+2015G>T MANE Select NP_000518.1:n.67+2015G>T
NM_001195798.2:c.67+2015G>T NP_001182727.1:n.67+2015G>T
NM_001195799.2:c.67+2015G>T NP_001182728.1:n.67+2015G>T
NM_001195800.2:c.67+2015G>T NP_001182729.1:n.67+2015G>T
NM_001195803.2:c.67+2015G>T NP_001182732.1:n.67+2015G>T