Canonical Allele Identifier: CA2322775391
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120160T= , CM000681.2:g.11120160T= GRCh38
NC_000019.9:g.11230836T= , CM000681.1:g.11230836T= GRCh37
NC_000019.8:g.11091836T= NCBI36
NG_009060.1:g.35780T= , LRG_274:g.35780T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2172T= ENSP00000252444.6:p.Asp724=
ENST00000559340.2:c.1774T= ENSP00000453696.2:p.Cys592=
ENST00000560467.2:c.1794T= ENSP00000453513.2:p.Asp598=
ENST00000558518.6:c.1914T= MANE Select ENSP00000454071.1:p.Asp638=
ENST00000252444.9:c.2168T=
ENST00000455727.6:c.1410T= ENSP00000397829.2:p.Asp470=
ENST00000535915.5:c.1791T= ENSP00000440520.1:p.Asp597=
ENST00000545707.5:c.1533T= ENSP00000437639.1:p.Asp511=
ENST00000557933.5:c.1914T= ENSP00000453557.1:p.Asp638=
ENST00000558013.5:c.1914T= ENSP00000453346.1:p.Asp638=
ENST00000558518.5:c.1914T= ENSP00000454071.1:p.Asp638=
ENST00000559340.1:c.495T=
NM_000527.4:c.1914T= , LRG_274t1:c.1914T= NP_000518.1:p.Asp638=
NM_001195798.1:c.1914T= NP_001182727.1:p.Asp638=
NM_001195799.1:c.1791T= NP_001182728.1:p.Asp597=
NM_001195800.1:c.1410T= NP_001182729.1:p.Asp470=
NM_001195803.1:c.1533T= NP_001182732.1:p.Asp511=
XM_011528010.1:c.1914T= XP_011526312.1:p.Asp638=
XM_011528011.1:c.1533T= XP_011526313.1:p.Asp511=
XR_244074.2:n.1924T=
XM_011528010.2:c.1914T= XP_011526312.1:p.Asp638=
XR_001753685.2:n.2031T=
XR_001753686.2:n.1891T=
NM_000527.5:c.1914T= MANE Select NP_000518.1:p.Asp638=
NM_001195798.2:c.1914T= NP_001182727.1:p.Asp638=
NM_001195799.2:c.1791T= NP_001182728.1:p.Asp597=
NM_001195800.2:c.1410T= NP_001182729.1:p.Asp470=
NM_001195803.2:c.1533T= NP_001182732.1:p.Asp511=