Canonical Allele Identifier: CA036811
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 440665
dbSNP Id: rs143872778

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116989C>A , CM000681.2:g.11116989C>A GRCh38
NC_000019.9:g.11227665C>A , CM000681.1:g.11227665C>A GRCh37
NC_000019.8:g.11088665C>A NCBI36
NG_009060.1:g.32609C>A , LRG_274:g.32609C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2094C>A ENSP00000252444.6:p.Ala698=
ENST00000559340.2:c.1705+777C>A ENSP00000453696.2:n.1705+777C>A
ENST00000560467.2:c.1716C>A ENSP00000453513.2:p.Ala572=
ENST00000558518.6:c.1836C>A MANE Select ENSP00000454071.1:p.Ala612=
ENST00000252444.9:c.2090C>A
ENST00000455727.6:c.1332C>A ENSP00000397829.2:p.Ala444=
ENST00000535915.5:c.1713C>A ENSP00000440520.1:p.Ala571=
ENST00000545707.5:c.1455C>A ENSP00000437639.1:p.Ala485=
ENST00000557933.5:c.1836C>A ENSP00000453557.1:p.Ala612=
ENST00000558013.5:c.1836C>A ENSP00000453346.1:p.Ala612=
ENST00000558518.5:c.1836C>A ENSP00000454071.1:p.Ala612=
ENST00000559340.1:c.426+777C>A
NM_000527.4:c.1836C>A , LRG_274t1:c.1836C>A NP_000518.1:p.Ala612=
NM_001195798.1:c.1836C>A NP_001182727.1:p.Ala612=
NM_001195799.1:c.1713C>A NP_001182728.1:p.Ala571=
NM_001195800.1:c.1332C>A NP_001182729.1:p.Ala444=
NM_001195803.1:c.1455C>A NP_001182732.1:p.Ala485=
XM_011528010.1:c.1836C>A XP_011526312.1:p.Ala612=
XM_011528011.1:c.1455C>A XP_011526313.1:p.Ala485=
XR_244074.2:n.1855+777C>A
XM_011528010.2:c.1836C>A XP_011526312.1:p.Ala612=
XR_001753685.2:n.1953C>A
XR_001753686.2:n.1822+777C>A
NM_000527.5:c.1836C>A MANE Select NP_000518.1:p.Ala612=
NM_001195798.2:c.1836C>A NP_001182727.1:p.Ala612=
NM_001195799.2:c.1713C>A NP_001182728.1:p.Ala571=
NM_001195800.2:c.1332C>A NP_001182729.1:p.Ala444=
NM_001195803.2:c.1455C>A NP_001182732.1:p.Ala485=