Canonical Allele Identifier: CA10585631
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 252051
dbSNP Id: rs879255035

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116976C>T , CM000681.2:g.11116976C>T GRCh38
NC_000019.9:g.11227652C>T , CM000681.1:g.11227652C>T GRCh37
NC_000019.8:g.11088652C>T NCBI36
NG_009060.1:g.32596C>T , LRG_274:g.32596C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2081C>T ENSP00000252444.6:p.Pro694Leu
ENST00000559340.2:c.1705+764C>T ENSP00000453696.2:n.1705+764C>T
ENST00000560467.2:c.1703C>T ENSP00000453513.2:p.Pro568Leu
ENST00000558518.6:c.1823C>T MANE Select ENSP00000454071.1:p.Pro608Leu
ENST00000252444.9:c.2077C>T
ENST00000455727.6:c.1319C>T ENSP00000397829.2:p.Pro440Leu
ENST00000535915.5:c.1700C>T ENSP00000440520.1:p.Pro567Leu
ENST00000545707.5:c.1442C>T ENSP00000437639.1:p.Pro481Leu
ENST00000557933.5:c.1823C>T ENSP00000453557.1:p.Pro608Leu
ENST00000558013.5:c.1823C>T ENSP00000453346.1:p.Pro608Leu
ENST00000558518.5:c.1823C>T ENSP00000454071.1:p.Pro608Leu
ENST00000559340.1:c.426+764C>T
NM_000527.4:c.1823C>T , LRG_274t1:c.1823C>T NP_000518.1:p.Pro608Leu
NM_001195798.1:c.1823C>T NP_001182727.1:p.Pro608Leu
NM_001195799.1:c.1700C>T NP_001182728.1:p.Pro567Leu
NM_001195800.1:c.1319C>T NP_001182729.1:p.Pro440Leu
NM_001195803.1:c.1442C>T NP_001182732.1:p.Pro481Leu
XM_011528010.1:c.1823C>T XP_011526312.1:p.Pro608Leu
XM_011528011.1:c.1442C>T XP_011526313.1:p.Pro481Leu
XR_244074.2:n.1855+764C>T
XM_011528010.2:c.1823C>T XP_011526312.1:p.Pro608Leu
XR_001753685.2:n.1940C>T
XR_001753686.2:n.1822+764C>T
NM_000527.5:c.1823C>T MANE Select NP_000518.1:p.Pro608Leu
NM_001195798.2:c.1823C>T NP_001182727.1:p.Pro608Leu
NM_001195799.2:c.1700C>T NP_001182728.1:p.Pro567Leu
NM_001195800.2:c.1319C>T NP_001182729.1:p.Pro440Leu
NM_001195803.2:c.1442C>T NP_001182732.1:p.Pro481Leu