Canonical Allele Identifier: CA2322780324
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129653G= , CM000681.2:g.11129653G= GRCh38
NC_000019.9:g.11240329G= , CM000681.1:g.11240329G= GRCh37
NC_000019.8:g.11101329G= NCBI36
NG_009060.1:g.45273G= , LRG_274:g.45273G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2788G= ENSP00000252444.6:p.Gly930=
ENST00000559340.2:c.*599G= ENSP00000453696.2:n.*599G=
ENST00000560467.2:c.2410G= ENSP00000453513.2:p.Gly804=
ENST00000558518.6:c.2530G= MANE Select ENSP00000454071.1:p.Gly844=
ENST00000252444.9:c.2784G=
ENST00000455727.6:c.2026G= ENSP00000397829.2:p.Gly676=
ENST00000535915.5:c.2407G= ENSP00000440520.1:p.Gly803=
ENST00000545707.5:c.1996G= ENSP00000437639.1:p.Gly666=
ENST00000557933.5:c.2592G= ENSP00000453557.1:p.Thr864=
ENST00000558013.5:c.2530G= ENSP00000453346.1:p.Gly844=
ENST00000558518.5:c.2530G= ENSP00000454071.1:p.Gly844=
ENST00000560628.1:n.108+1999G=
NM_000527.4:c.2530G= , LRG_274t1:c.2530G= NP_000518.1:p.Gly844=
NM_001195798.1:c.2530G= NP_001182727.1:p.Gly844=
NM_001195799.1:c.2407G= NP_001182728.1:p.Gly803=
NM_001195800.1:c.2026G= NP_001182729.1:p.Gly676=
NM_001195803.1:c.1996G= NP_001182732.1:p.Gly666=
XM_011528010.1:c.2452G= XP_011526312.1:p.Gly818=
XM_011528011.1:c.2149G= XP_011526313.1:p.Gly717=
XM_011528010.2:c.2452G= XP_011526312.1:p.Gly818=
XR_001753685.2:n.2864G=
XR_001753686.2:n.2507G=
NM_000527.5:c.2530G= MANE Select NP_000518.1:p.Gly844=
NM_001195798.2:c.2530G= NP_001182727.1:p.Gly844=
NM_001195799.2:c.2407G= NP_001182728.1:p.Gly803=
NM_001195800.2:c.2026G= NP_001182729.1:p.Gly676=
NM_001195803.2:c.1996G= NP_001182732.1:p.Gly666=