Canonical Allele Identifier: CA2322767444
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105415A= , CM000681.2:g.11105415A= GRCh38
NC_000019.9:g.11216091A= , CM000681.1:g.11216091A= GRCh37
NC_000019.8:g.11077091A= NCBI36
NG_009060.1:g.21035A= , LRG_274:g.21035A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.767A= ENSP00000252444.6:p.Asp256=
ENST00000559340.2:c.509A= ENSP00000453696.2:p.Asp170=
ENST00000560467.2:c.509A= ENSP00000453513.2:p.Asp170=
ENST00000558518.6:c.509A= MANE Select ENSP00000454071.1:p.Asp170=
ENST00000252444.9:c.763A=
ENST00000455727.6:c.314-1977A= ENSP00000397829.2:n.314-1977A=
ENST00000535915.5:c.386A= ENSP00000440520.1:p.Asp129=
ENST00000545707.5:c.314-1150A= ENSP00000437639.1:n.314-1150A=
ENST00000557933.5:c.509A= ENSP00000453557.1:p.Asp170=
ENST00000558013.5:c.509A= ENSP00000453346.1:p.Asp170=
ENST00000558518.5:c.509A= ENSP00000454071.1:p.Asp170=
ENST00000560467.1:c.109A=
NM_000527.4:c.509A= , LRG_274t1:c.509A= NP_000518.1:p.Asp170=
NM_001195798.1:c.509A= NP_001182727.1:p.Asp170=
NM_001195799.1:c.386A= NP_001182728.1:p.Asp129=
NM_001195800.1:c.314-1977A= NP_001182729.1:n.314-1977A=
NM_001195803.1:c.314-1150A= NP_001182732.1:n.314-1150A=
XM_011528010.1:c.509A= XP_011526312.1:p.Asp170=
XM_011528011.1:c.314-1150A= XP_011526313.1:n.314-1150A=
XR_244074.2:n.659A=
XM_011528010.2:c.509A= XP_011526312.1:p.Asp170=
XR_001753685.2:n.626A=
XR_001753686.2:n.626A=
NM_000527.5:c.509A= MANE Select NP_000518.1:p.Asp170=
NM_001195798.2:c.509A= NP_001182727.1:p.Asp170=
NM_001195799.2:c.386A= NP_001182728.1:p.Asp129=
NM_001195800.2:c.314-1977A= NP_001182729.1:n.314-1977A=
NM_001195803.2:c.314-1150A= NP_001182732.1:n.314-1150A=