Canonical Allele Identifier: CA2322768644
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107494A= , CM000681.2:g.11107494A= GRCh38
NC_000019.9:g.11218170A= , CM000681.1:g.11218170A= GRCh37
NC_000019.8:g.11079170A= NCBI36
NG_009060.1:g.23114A= , LRG_274:g.23114A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1178A= ENSP00000252444.6:p.Asp393=
ENST00000559340.2:c.920A= ENSP00000453696.2:p.Asp307=
ENST00000560467.2:c.920A= ENSP00000453513.2:p.Asp307=
ENST00000558518.6:c.920A= MANE Select ENSP00000454071.1:p.Asp307=
ENST00000252444.9:c.1174A=
ENST00000455727.6:c.416A= ENSP00000397829.2:p.Asp139=
ENST00000535915.5:c.797A= ENSP00000440520.1:p.Asp266=
ENST00000545707.5:c.539A= ENSP00000437639.1:p.Asp180=
ENST00000557933.5:c.920A= ENSP00000453557.1:p.Asp307=
ENST00000558013.5:c.920A= ENSP00000453346.1:p.Asp307=
ENST00000558518.5:c.920A= ENSP00000454071.1:p.Asp307=
ENST00000558528.1:n.435A=
ENST00000560467.1:c.520A=
NM_000527.4:c.920A= , LRG_274t1:c.920A= NP_000518.1:p.Asp307=
NM_001195798.1:c.920A= NP_001182727.1:p.Asp307=
NM_001195799.1:c.797A= NP_001182728.1:p.Asp266=
NM_001195800.1:c.416A= NP_001182729.1:p.Asp139=
NM_001195803.1:c.539A= NP_001182732.1:p.Asp180=
XM_011528010.1:c.920A= XP_011526312.1:p.Asp307=
XM_011528011.1:c.539A= XP_011526313.1:p.Asp180=
XR_244074.2:n.1070A=
XM_011528010.2:c.920A= XP_011526312.1:p.Asp307=
XR_001753685.2:n.1037A=
XR_001753686.2:n.1037A=
NM_000527.5:c.920A= MANE Select NP_000518.1:p.Asp307=
NM_001195798.2:c.920A= NP_001182727.1:p.Asp307=
NM_001195799.2:c.797A= NP_001182728.1:p.Asp266=
NM_001195800.2:c.416A= NP_001182729.1:p.Asp139=
NM_001195803.2:c.539A= NP_001182732.1:p.Asp180=