Canonical Allele Identifier: CA2322780310
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129623G= , CM000681.2:g.11129623G= GRCh38
NC_000019.9:g.11240299G= , CM000681.1:g.11240299G= GRCh37
NC_000019.8:g.11101299G= NCBI36
NG_009060.1:g.45243G= , LRG_274:g.45243G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2758G= ENSP00000252444.6:p.Asp920=
ENST00000559340.2:c.*569G= ENSP00000453696.2:n.*569G=
ENST00000560467.2:c.2380G= ENSP00000453513.2:p.Asp794=
ENST00000558518.6:c.2500G= MANE Select ENSP00000454071.1:p.Asp834=
ENST00000252444.9:c.2754G=
ENST00000455727.6:c.1996G= ENSP00000397829.2:p.Asp666=
ENST00000535915.5:c.2377G= ENSP00000440520.1:p.Asp793=
ENST00000545707.5:c.1966G= ENSP00000437639.1:p.Asp656=
ENST00000557933.5:c.2562G= ENSP00000453557.1:p.Arg854=
ENST00000558013.5:c.2500G= ENSP00000453346.1:p.Asp834=
ENST00000558518.5:c.2500G= ENSP00000454071.1:p.Asp834=
ENST00000560628.1:n.108+1969G=
NM_000527.4:c.2500G= , LRG_274t1:c.2500G= NP_000518.1:p.Asp834=
NM_001195798.1:c.2500G= NP_001182727.1:p.Asp834=
NM_001195799.1:c.2377G= NP_001182728.1:p.Asp793=
NM_001195800.1:c.1996G= NP_001182729.1:p.Asp666=
NM_001195803.1:c.1966G= NP_001182732.1:p.Asp656=
XM_011528010.1:c.2422G= XP_011526312.1:p.Asp808=
XM_011528011.1:c.2119G= XP_011526313.1:p.Asp707=
XM_011528010.2:c.2422G= XP_011526312.1:p.Asp808=
XR_001753685.2:n.2834G=
XR_001753686.2:n.2477G=
NM_000527.5:c.2500G= MANE Select NP_000518.1:p.Asp834=
NM_001195798.2:c.2500G= NP_001182727.1:p.Asp834=
NM_001195799.2:c.2377G= NP_001182728.1:p.Asp793=
NM_001195800.2:c.1996G= NP_001182729.1:p.Asp666=
NM_001195803.2:c.1966G= NP_001182732.1:p.Asp656=