Canonical Allele Identifier: CA404098318
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129525T>A , CM000681.2:g.11129525T>A GRCh38
NC_000019.9:g.11240201T>A , CM000681.1:g.11240201T>A GRCh37
NC_000019.8:g.11101201T>A NCBI36
NG_009060.1:g.45145T>A , LRG_274:g.45145T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2660T>A ENSP00000252444.6:p.Phe887Tyr
ENST00000559340.2:c.*471T>A ENSP00000453696.2:n.*471T>A
ENST00000560467.2:c.2282T>A ENSP00000453513.2:p.Phe761Tyr
ENST00000558518.6:c.2402T>A MANE Select ENSP00000454071.1:p.Phe801Tyr
ENST00000252444.9:c.2656T>A
ENST00000455727.6:c.1898T>A ENSP00000397829.2:p.Phe633Tyr
ENST00000535915.5:c.2279T>A ENSP00000440520.1:p.Phe760Tyr
ENST00000545707.5:c.1868T>A ENSP00000437639.1:p.Phe623Tyr
ENST00000557933.5:c.2464T>A ENSP00000453557.1:p.Ser822Thr
ENST00000558013.5:c.2402T>A ENSP00000453346.1:p.Phe801Tyr
ENST00000558518.5:c.2402T>A ENSP00000454071.1:p.Phe801Tyr
ENST00000560628.1:n.108+1871T>A
NM_000527.4:c.2402T>A , LRG_274t1:c.2402T>A NP_000518.1:p.Phe801Tyr
NM_001195798.1:c.2402T>A NP_001182727.1:p.Phe801Tyr
NM_001195799.1:c.2279T>A NP_001182728.1:p.Phe760Tyr
NM_001195800.1:c.1898T>A NP_001182729.1:p.Phe633Tyr
NM_001195803.1:c.1868T>A NP_001182732.1:p.Phe623Tyr
XM_011528010.1:c.2324T>A XP_011526312.1:p.Phe775Tyr
XM_011528011.1:c.2021T>A XP_011526313.1:p.Phe674Tyr
XR_244074.2:n.2412T>A
XM_011528010.2:c.2324T>A XP_011526312.1:p.Phe775Tyr
XR_001753685.2:n.2736T>A
XR_001753686.2:n.2379T>A
NM_000527.5:c.2402T>A MANE Select NP_000518.1:p.Phe801Tyr
NM_001195798.2:c.2402T>A NP_001182727.1:p.Phe801Tyr
NM_001195799.2:c.2279T>A NP_001182728.1:p.Phe760Tyr
NM_001195800.2:c.1898T>A NP_001182729.1:p.Phe633Tyr
NM_001195803.2:c.1868T>A NP_001182732.1:p.Phe623Tyr