Canonical Allele Identifier: CA2322770253
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110697G= , CM000681.2:g.11110697G= GRCh38
NC_000019.9:g.11221373G= , CM000681.1:g.11221373G= GRCh37
NC_000019.8:g.11082373G= NCBI36
NG_009060.1:g.26317G= , LRG_274:g.26317G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1244G= ENSP00000252444.6:p.Cys415=
ENST00000559340.2:c.986G= ENSP00000453696.2:p.Cys329=
ENST00000560467.2:c.941-817G= ENSP00000453513.2:n.941-817G=
ENST00000558518.6:c.986G= MANE Select ENSP00000454071.1:p.Cys329=
ENST00000252444.9:c.1240G=
ENST00000455727.6:c.482G= ENSP00000397829.2:p.Cys161=
ENST00000535915.5:c.863G= ENSP00000440520.1:p.Cys288=
ENST00000545707.5:c.605G= ENSP00000437639.1:p.Cys202=
ENST00000557933.5:c.986G= ENSP00000453557.1:p.Cys329=
ENST00000558013.5:c.986G= ENSP00000453346.1:p.Cys329=
ENST00000558518.5:c.986G= ENSP00000454071.1:p.Cys329=
ENST00000560467.1:c.541-817G=
NM_000527.4:c.986G= , LRG_274t1:c.986G= NP_000518.1:p.Cys329=
NM_001195798.1:c.986G= NP_001182727.1:p.Cys329=
NM_001195799.1:c.863G= NP_001182728.1:p.Cys288=
NM_001195800.1:c.482G= NP_001182729.1:p.Cys161=
NM_001195803.1:c.605G= NP_001182732.1:p.Cys202=
XM_011528010.1:c.986G= XP_011526312.1:p.Cys329=
XM_011528011.1:c.605G= XP_011526313.1:p.Cys202=
XR_244074.2:n.1136G=
XM_011528010.2:c.986G= XP_011526312.1:p.Cys329=
XR_001753685.2:n.1103G=
XR_001753686.2:n.1103G=
NM_000527.5:c.986G= MANE Select NP_000518.1:p.Cys329=
NM_001195798.2:c.986G= NP_001182727.1:p.Cys329=
NM_001195799.2:c.863G= NP_001182728.1:p.Cys288=
NM_001195800.2:c.482G= NP_001182729.1:p.Cys161=
NM_001195803.2:c.605G= NP_001182732.1:p.Cys202=