Canonical Allele Identifier: CA2322780262
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129534T= , CM000681.2:g.11129534T= GRCh38
NC_000019.9:g.11240210T= , CM000681.1:g.11240210T= GRCh37
NC_000019.8:g.11101210T= NCBI36
NG_009060.1:g.45154T= , LRG_274:g.45154T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2669T= ENSP00000252444.6:p.Leu890=
ENST00000559340.2:c.*480T= ENSP00000453696.2:n.*480T=
ENST00000560467.2:c.2291T= ENSP00000453513.2:p.Leu764=
ENST00000558518.6:c.2411T= MANE Select ENSP00000454071.1:p.Leu804=
ENST00000252444.9:c.2665T=
ENST00000455727.6:c.1907T= ENSP00000397829.2:p.Leu636=
ENST00000535915.5:c.2288T= ENSP00000440520.1:p.Leu763=
ENST00000545707.5:c.1877T= ENSP00000437639.1:p.Leu626=
ENST00000557933.5:c.2473T= ENSP00000453557.1:p.Trp825=
ENST00000558013.5:c.2411T= ENSP00000453346.1:p.Leu804=
ENST00000558518.5:c.2411T= ENSP00000454071.1:p.Leu804=
ENST00000560628.1:n.108+1880T=
NM_000527.4:c.2411T= , LRG_274t1:c.2411T= NP_000518.1:p.Leu804=
NM_001195798.1:c.2411T= NP_001182727.1:p.Leu804=
NM_001195799.1:c.2288T= NP_001182728.1:p.Leu763=
NM_001195800.1:c.1907T= NP_001182729.1:p.Leu636=
NM_001195803.1:c.1877T= NP_001182732.1:p.Leu626=
XM_011528010.1:c.2333T= XP_011526312.1:p.Leu778=
XM_011528011.1:c.2030T= XP_011526313.1:p.Leu677=
XR_244074.2:n.2421T=
XM_011528010.2:c.2333T= XP_011526312.1:p.Leu778=
XR_001753685.2:n.2745T=
XR_001753686.2:n.2388T=
NM_000527.5:c.2411T= MANE Select NP_000518.1:p.Leu804=
NM_001195798.2:c.2411T= NP_001182727.1:p.Leu804=
NM_001195799.2:c.2288T= NP_001182728.1:p.Leu763=
NM_001195800.2:c.1907T= NP_001182729.1:p.Leu636=
NM_001195803.2:c.1877T= NP_001182732.1:p.Leu626=