Canonical Allele Identifier: CA404092420
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 1379706
ClinVar RCV Id: RCV001883908
dbSNP Id: rs879255058

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120108C>T , CM000681.2:g.11120108C>T GRCh38
NC_000019.9:g.11230784C>T , CM000681.1:g.11230784C>T GRCh37
NC_000019.8:g.11091784C>T NCBI36
NG_009060.1:g.35728C>T , LRG_274:g.35728C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2120C>T ENSP00000252444.6:p.Thr707Ile
ENST00000559340.2:c.1722C>T ENSP00000453696.2:p.Asp574=
ENST00000560467.2:c.1742C>T ENSP00000453513.2:p.Thr581Ile
ENST00000558518.6:c.1862C>T MANE Select ENSP00000454071.1:p.Thr621Ile
ENST00000252444.9:c.2116C>T
ENST00000455727.6:c.1358C>T ENSP00000397829.2:p.Thr453Ile
ENST00000535915.5:c.1739C>T ENSP00000440520.1:p.Thr580Ile
ENST00000545707.5:c.1481C>T ENSP00000437639.1:p.Thr494Ile
ENST00000557933.5:c.1862C>T ENSP00000453557.1:p.Thr621Ile
ENST00000558013.5:c.1862C>T ENSP00000453346.1:p.Thr621Ile
ENST00000558518.5:c.1862C>T ENSP00000454071.1:p.Thr621Ile
ENST00000559340.1:c.443C>T
NM_000527.4:c.1862C>T , LRG_274t1:c.1862C>T NP_000518.1:p.Thr621Ile
NM_001195798.1:c.1862C>T NP_001182727.1:p.Thr621Ile
NM_001195799.1:c.1739C>T NP_001182728.1:p.Thr580Ile
NM_001195800.1:c.1358C>T NP_001182729.1:p.Thr453Ile
NM_001195803.1:c.1481C>T NP_001182732.1:p.Thr494Ile
XM_011528010.1:c.1862C>T XP_011526312.1:p.Thr621Ile
XM_011528011.1:c.1481C>T XP_011526313.1:p.Thr494Ile
XR_244074.2:n.1872C>T
XM_011528010.2:c.1862C>T XP_011526312.1:p.Thr621Ile
XR_001753685.2:n.1979C>T
XR_001753686.2:n.1839C>T
NM_000527.5:c.1862C>T MANE Select NP_000518.1:p.Thr621Ile
NM_001195798.2:c.1862C>T NP_001182727.1:p.Thr621Ile
NM_001195799.2:c.1739C>T NP_001182728.1:p.Thr580Ile
NM_001195800.2:c.1358C>T NP_001182729.1:p.Thr453Ile
NM_001195803.2:c.1481C>T NP_001182732.1:p.Thr494Ile