Canonical Allele Identifier: CA2322777277
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123342A= , CM000681.2:g.11123342A= GRCh38
NC_000019.9:g.11234018A= , CM000681.1:g.11234018A= GRCh37
NC_000019.8:g.11095018A= NCBI36
NG_009060.1:g.38962A= , LRG_274:g.38962A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2567A= ENSP00000252444.6:p.Gln856=
ENST00000559340.2:c.*378A= ENSP00000453696.2:n.*378A=
ENST00000560467.2:c.2189A= ENSP00000453513.2:p.Gln730=
ENST00000558518.6:c.2309A= MANE Select ENSP00000454071.1:p.Gln770=
ENST00000252444.9:c.2563A=
ENST00000455727.6:c.1805A= ENSP00000397829.2:p.Gln602=
ENST00000535915.5:c.2186A= ENSP00000440520.1:p.Gln729=
ENST00000545707.5:c.1775A= ENSP00000437639.1:p.Gln592=
ENST00000557933.5:c.2309A= ENSP00000453557.1:p.Gln770=
ENST00000558013.5:c.2309A= ENSP00000453346.1:p.Gln770=
ENST00000558518.5:c.2309A= ENSP00000454071.1:p.Gln770=
NM_000527.4:c.2309A= , LRG_274t1:c.2309A= NP_000518.1:p.Gln770=
NM_001195798.1:c.2309A= NP_001182727.1:p.Gln770=
NM_001195799.1:c.2186A= NP_001182728.1:p.Gln729=
NM_001195800.1:c.1805A= NP_001182729.1:p.Gln602=
NM_001195803.1:c.1775A= NP_001182732.1:p.Gln592=
XM_011528010.1:c.2309A= XP_011526312.1:p.Gln770=
XM_011528011.1:c.1928A= XP_011526313.1:p.Gln643=
XR_244074.2:n.2319A=
XM_011528010.2:c.2309A= XP_011526312.1:p.Gln770=
XR_001753685.2:n.2643A=
XR_001753686.2:n.2286A=
NM_000527.5:c.2309A= MANE Select NP_000518.1:p.Gln770=
NM_001195798.2:c.2309A= NP_001182727.1:p.Gln770=
NM_001195799.2:c.2186A= NP_001182728.1:p.Gln729=
NM_001195800.2:c.1805A= NP_001182729.1:p.Gln602=
NM_001195803.2:c.1775A= NP_001182732.1:p.Gln592=