Canonical Allele Identifier: CA2322770241
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110684T= , CM000681.2:g.11110684T= GRCh38
NC_000019.9:g.11221360T= , CM000681.1:g.11221360T= GRCh37
NC_000019.8:g.11082360T= NCBI36
NG_009060.1:g.26304T= , LRG_274:g.26304T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1231T= ENSP00000252444.6:p.Cys411=
ENST00000559340.2:c.973T= ENSP00000453696.2:p.Cys325=
ENST00000560467.2:c.941-830T= ENSP00000453513.2:n.941-830T=
ENST00000558518.6:c.973T= MANE Select ENSP00000454071.1:p.Cys325=
ENST00000252444.9:c.1227T=
ENST00000455727.6:c.469T= ENSP00000397829.2:p.Cys157=
ENST00000535915.5:c.850T= ENSP00000440520.1:p.Cys284=
ENST00000545707.5:c.592T= ENSP00000437639.1:p.Cys198=
ENST00000557933.5:c.973T= ENSP00000453557.1:p.Cys325=
ENST00000558013.5:c.973T= ENSP00000453346.1:p.Cys325=
ENST00000558518.5:c.973T= ENSP00000454071.1:p.Cys325=
ENST00000560467.1:c.541-830T=
NM_000527.4:c.973T= , LRG_274t1:c.973T= NP_000518.1:p.Cys325=
NM_001195798.1:c.973T= NP_001182727.1:p.Cys325=
NM_001195799.1:c.850T= NP_001182728.1:p.Cys284=
NM_001195800.1:c.469T= NP_001182729.1:p.Cys157=
NM_001195803.1:c.592T= NP_001182732.1:p.Cys198=
XM_011528010.1:c.973T= XP_011526312.1:p.Cys325=
XM_011528011.1:c.592T= XP_011526313.1:p.Cys198=
XR_244074.2:n.1123T=
XM_011528010.2:c.973T= XP_011526312.1:p.Cys325=
XR_001753685.2:n.1090T=
XR_001753686.2:n.1090T=
NM_000527.5:c.973T= MANE Select NP_000518.1:p.Cys325=
NM_001195798.2:c.973T= NP_001182727.1:p.Cys325=
NM_001195799.2:c.850T= NP_001182728.1:p.Cys284=
NM_001195800.2:c.469T= NP_001182729.1:p.Cys157=
NM_001195803.2:c.592T= NP_001182732.1:p.Cys198=