Canonical Allele Identifier: CA2322767441
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105412A= , CM000681.2:g.11105412A= GRCh38
NC_000019.9:g.11216088A= , CM000681.1:g.11216088A= GRCh37
NC_000019.8:g.11077088A= NCBI36
NG_009060.1:g.21032A= , LRG_274:g.21032A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.764A= ENSP00000252444.6:p.Asn255=
ENST00000559340.2:c.506A= ENSP00000453696.2:p.Asn169=
ENST00000560467.2:c.506A= ENSP00000453513.2:p.Asn169=
ENST00000558518.6:c.506A= MANE Select ENSP00000454071.1:p.Asn169=
ENST00000252444.9:c.760A=
ENST00000455727.6:c.314-1980A= ENSP00000397829.2:n.314-1980A=
ENST00000535915.5:c.383A= ENSP00000440520.1:p.Asn128=
ENST00000545707.5:c.314-1153A= ENSP00000437639.1:n.314-1153A=
ENST00000557933.5:c.506A= ENSP00000453557.1:p.Asn169=
ENST00000558013.5:c.506A= ENSP00000453346.1:p.Asn169=
ENST00000558518.5:c.506A= ENSP00000454071.1:p.Asn169=
ENST00000560467.1:c.106A=
NM_000527.4:c.506A= , LRG_274t1:c.506A= NP_000518.1:p.Asn169=
NM_001195798.1:c.506A= NP_001182727.1:p.Asn169=
NM_001195799.1:c.383A= NP_001182728.1:p.Asn128=
NM_001195800.1:c.314-1980A= NP_001182729.1:n.314-1980A=
NM_001195803.1:c.314-1153A= NP_001182732.1:n.314-1153A=
XM_011528010.1:c.506A= XP_011526312.1:p.Asn169=
XM_011528011.1:c.314-1153A= XP_011526313.1:n.314-1153A=
XR_244074.2:n.656A=
XM_011528010.2:c.506A= XP_011526312.1:p.Asn169=
XR_001753685.2:n.623A=
XR_001753686.2:n.623A=
NM_000527.5:c.506A= MANE Select NP_000518.1:p.Asn169=
NM_001195798.2:c.506A= NP_001182727.1:p.Asn169=
NM_001195799.2:c.383A= NP_001182728.1:p.Asn128=
NM_001195800.2:c.314-1980A= NP_001182729.1:n.314-1980A=
NM_001195803.2:c.314-1153A= NP_001182732.1:n.314-1153A=