Canonical Allele Identifier: CA404085008
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113386T>A , CM000681.2:g.11113386T>A GRCh38
NC_000019.9:g.11224062T>A , CM000681.1:g.11224062T>A GRCh37
NC_000019.8:g.11085062T>A NCBI36
NG_009060.1:g.29006T>A , LRG_274:g.29006T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1553T>A ENSP00000252444.6:p.Leu518Gln
ENST00000559340.2:c.1295T>A ENSP00000453696.2:p.Leu432Gln
ENST00000560467.2:c.1175T>A ENSP00000453513.2:p.Leu392Gln
ENST00000558518.6:c.1295T>A MANE Select ENSP00000454071.1:p.Leu432Gln
ENST00000252444.9:c.1549T>A
ENST00000455727.6:c.791T>A ENSP00000397829.2:p.Leu264Gln
ENST00000535915.5:c.1172T>A ENSP00000440520.1:p.Leu391Gln
ENST00000545707.5:c.914T>A ENSP00000437639.1:p.Leu305Gln
ENST00000557933.5:c.1295T>A ENSP00000453557.1:p.Leu432Gln
ENST00000558013.5:c.1295T>A ENSP00000453346.1:p.Leu432Gln
ENST00000558518.5:c.1295T>A ENSP00000454071.1:p.Leu432Gln
ENST00000559340.1:c.16T>A
ENST00000560173.1:n.294T>A
ENST00000560467.1:c.775T>A
NM_000527.4:c.1295T>A , LRG_274t1:c.1295T>A NP_000518.1:p.Leu432Gln
NM_001195798.1:c.1295T>A NP_001182727.1:p.Leu432Gln
NM_001195799.1:c.1172T>A NP_001182728.1:p.Leu391Gln
NM_001195800.1:c.791T>A NP_001182729.1:p.Leu264Gln
NM_001195803.1:c.914T>A NP_001182732.1:p.Leu305Gln
XM_011528010.1:c.1295T>A XP_011526312.1:p.Leu432Gln
XM_011528011.1:c.914T>A XP_011526313.1:p.Leu305Gln
XR_244074.2:n.1445T>A
XM_011528010.2:c.1295T>A XP_011526312.1:p.Leu432Gln
XR_001753685.2:n.1412T>A
XR_001753686.2:n.1412T>A
NM_000527.5:c.1295T>A MANE Select NP_000518.1:p.Leu432Gln
NM_001195798.2:c.1295T>A NP_001182727.1:p.Leu432Gln
NM_001195799.2:c.1172T>A NP_001182728.1:p.Leu391Gln
NM_001195800.2:c.791T>A NP_001182729.1:p.Leu264Gln
NM_001195803.2:c.914T>A NP_001182732.1:p.Leu305Gln