Canonical Allele Identifier: CA404096906
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128079C>T , CM000681.2:g.11128079C>T GRCh38
NC_000019.9:g.11238755C>T , CM000681.1:g.11238755C>T GRCh37
NC_000019.8:g.11099755C>T NCBI36
NG_009060.1:g.43699C>T , LRG_274:g.43699C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2641C>T ENSP00000252444.6:p.Pro881Ser
ENST00000559340.2:c.*452C>T ENSP00000453696.2:n.*452C>T
ENST00000560467.2:c.2263C>T ENSP00000453513.2:p.Pro755Ser
ENST00000558518.6:c.2383C>T MANE Select ENSP00000454071.1:p.Pro795Ser
ENST00000252444.9:c.2637C>T
ENST00000455727.6:c.1879C>T ENSP00000397829.2:p.Pro627Ser
ENST00000535915.5:c.2260C>T ENSP00000440520.1:p.Pro754Ser
ENST00000545707.5:c.1849C>T ENSP00000437639.1:p.Pro617Ser
ENST00000557933.5:c.2383C>T ENSP00000453557.1:p.Pro795Ser
ENST00000558013.5:c.2383C>T ENSP00000453346.1:p.Pro795Ser
ENST00000558518.5:c.2383C>T ENSP00000454071.1:p.Pro795Ser
ENST00000560628.1:n.108+425C>T
NM_000527.4:c.2383C>T , LRG_274t1:c.2383C>T NP_000518.1:p.Pro795Ser
NM_001195798.1:c.2383C>T NP_001182727.1:p.Pro795Ser
NM_001195799.1:c.2260C>T NP_001182728.1:p.Pro754Ser
NM_001195800.1:c.1879C>T NP_001182729.1:p.Pro627Ser
NM_001195803.1:c.1849C>T NP_001182732.1:p.Pro617Ser
XM_011528010.1:c.2312-1434C>T XP_011526312.1:n.2312-1434C>T
XM_011528011.1:c.2002C>T XP_011526313.1:p.Pro668Ser
XR_244074.2:n.2393C>T
XM_011528010.2:c.2312-1434C>T XP_011526312.1:n.2312-1434C>T
XR_001753685.2:n.2717C>T
XR_001753686.2:n.2360C>T
NM_000527.5:c.2383C>T MANE Select NP_000518.1:p.Pro795Ser
NM_001195798.2:c.2383C>T NP_001182727.1:p.Pro795Ser
NM_001195799.2:c.2260C>T NP_001182728.1:p.Pro754Ser
NM_001195800.2:c.1879C>T NP_001182729.1:p.Pro627Ser
NM_001195803.2:c.1849C>T NP_001182732.1:p.Pro617Ser