Canonical Allele Identifier: CA2322771689
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113291C= , CM000681.2:g.11113291C= GRCh38
NC_000019.9:g.11223967C= , CM000681.1:g.11223967C= GRCh37
NC_000019.8:g.11084967C= NCBI36
NG_009060.1:g.28911C= , LRG_274:g.28911C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1458C= ENSP00000252444.6:p.Tyr486=
ENST00000559340.2:c.1200C= ENSP00000453696.2:p.Tyr400=
ENST00000560467.2:c.1080C= ENSP00000453513.2:p.Tyr360=
ENST00000558518.6:c.1200C= MANE Select ENSP00000454071.1:p.Tyr400=
ENST00000252444.9:c.1454C=
ENST00000455727.6:c.696C= ENSP00000397829.2:p.Tyr232=
ENST00000535915.5:c.1077C= ENSP00000440520.1:p.Tyr359=
ENST00000545707.5:c.819C= ENSP00000437639.1:p.Tyr273=
ENST00000557933.5:c.1200C= ENSP00000453557.1:p.Tyr400=
ENST00000558013.5:c.1200C= ENSP00000453346.1:p.Tyr400=
ENST00000558518.5:c.1200C= ENSP00000454071.1:p.Tyr400=
ENST00000560173.1:n.199C=
ENST00000560467.1:c.680C=
NM_000527.4:c.1200C= , LRG_274t1:c.1200C= NP_000518.1:p.Tyr400=
NM_001195798.1:c.1200C= NP_001182727.1:p.Tyr400=
NM_001195799.1:c.1077C= NP_001182728.1:p.Tyr359=
NM_001195800.1:c.696C= NP_001182729.1:p.Tyr232=
NM_001195803.1:c.819C= NP_001182732.1:p.Tyr273=
XM_011528010.1:c.1200C= XP_011526312.1:p.Tyr400=
XM_011528011.1:c.819C= XP_011526313.1:p.Tyr273=
XR_244074.2:n.1350C=
XM_011528010.2:c.1200C= XP_011526312.1:p.Tyr400=
XR_001753685.2:n.1317C=
XR_001753686.2:n.1317C=
NM_000527.5:c.1200C= MANE Select NP_000518.1:p.Tyr400=
NM_001195798.2:c.1200C= NP_001182727.1:p.Tyr400=
NM_001195799.2:c.1077C= NP_001182728.1:p.Tyr359=
NM_001195800.2:c.696C= NP_001182729.1:p.Tyr232=
NM_001195803.2:c.819C= NP_001182732.1:p.Tyr273=