Canonical Allele Identifier: CA039712
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 630376
dbSNP Id: rs377563758

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128015C>T , CM000681.2:g.11128015C>T GRCh38
NC_000019.9:g.11238691C>T , CM000681.1:g.11238691C>T GRCh37
NC_000019.8:g.11099691C>T NCBI36
NG_009060.1:g.43635C>T , LRG_274:g.43635C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2577C>T ENSP00000252444.6:p.Gly859=
ENST00000559340.2:c.*388C>T ENSP00000453696.2:n.*388C>T
ENST00000560467.2:c.2199C>T ENSP00000453513.2:p.Gly733=
ENST00000558518.6:c.2319C>T MANE Select ENSP00000454071.1:p.Gly773=
ENST00000252444.9:c.2573C>T
ENST00000455727.6:c.1815C>T ENSP00000397829.2:p.Gly605=
ENST00000535915.5:c.2196C>T ENSP00000440520.1:p.Gly732=
ENST00000545707.5:c.1785C>T ENSP00000437639.1:p.Gly595=
ENST00000557933.5:c.2319C>T ENSP00000453557.1:p.Gly773=
ENST00000558013.5:c.2319C>T ENSP00000453346.1:p.Gly773=
ENST00000558518.5:c.2319C>T ENSP00000454071.1:p.Gly773=
ENST00000560628.1:n.108+361C>T
NM_000527.4:c.2319C>T , LRG_274t1:c.2319C>T NP_000518.1:p.Gly773=
NM_001195798.1:c.2319C>T NP_001182727.1:p.Gly773=
NM_001195799.1:c.2196C>T NP_001182728.1:p.Gly732=
NM_001195800.1:c.1815C>T NP_001182729.1:p.Gly605=
NM_001195803.1:c.1785C>T NP_001182732.1:p.Gly595=
XM_011528010.1:c.2312-1498C>T XP_011526312.1:n.2312-1498C>T
XM_011528011.1:c.1938C>T XP_011526313.1:p.Gly646=
XR_244074.2:n.2329C>T
XM_011528010.2:c.2312-1498C>T XP_011526312.1:n.2312-1498C>T
XR_001753685.2:n.2653C>T
XR_001753686.2:n.2296C>T
NM_000527.5:c.2319C>T MANE Select NP_000518.1:p.Gly773=
NM_001195798.2:c.2319C>T NP_001182727.1:p.Gly773=
NM_001195799.2:c.2196C>T NP_001182728.1:p.Gly732=
NM_001195800.2:c.1815C>T NP_001182729.1:p.Gly605=
NM_001195803.2:c.1785C>T NP_001182732.1:p.Gly595=