Canonical Allele Identifier: CA2322780322
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129646C= , CM000681.2:g.11129646C= GRCh38
NC_000019.9:g.11240322C= , CM000681.1:g.11240322C= GRCh37
NC_000019.8:g.11101322C= NCBI36
NG_009060.1:g.45266C= , LRG_274:g.45266C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2781C= ENSP00000252444.6:p.Asn927=
ENST00000559340.2:c.*592C= ENSP00000453696.2:n.*592C=
ENST00000560467.2:c.2403C= ENSP00000453513.2:p.Asn801=
ENST00000558518.6:c.2523C= MANE Select ENSP00000454071.1:p.Asn841=
ENST00000252444.9:c.2777C=
ENST00000455727.6:c.2019C= ENSP00000397829.2:p.Asn673=
ENST00000535915.5:c.2400C= ENSP00000440520.1:p.Asn800=
ENST00000545707.5:c.1989C= ENSP00000437639.1:p.Asn663=
ENST00000557933.5:c.2585C= ENSP00000453557.1:p.Thr862=
ENST00000558013.5:c.2523C= ENSP00000453346.1:p.Asn841=
ENST00000558518.5:c.2523C= ENSP00000454071.1:p.Asn841=
ENST00000560628.1:n.108+1992C=
NM_000527.4:c.2523C= , LRG_274t1:c.2523C= NP_000518.1:p.Asn841=
NM_001195798.1:c.2523C= NP_001182727.1:p.Asn841=
NM_001195799.1:c.2400C= NP_001182728.1:p.Asn800=
NM_001195800.1:c.2019C= NP_001182729.1:p.Asn673=
NM_001195803.1:c.1989C= NP_001182732.1:p.Asn663=
XM_011528010.1:c.2445C= XP_011526312.1:p.Asn815=
XM_011528011.1:c.2142C= XP_011526313.1:p.Asn714=
XM_011528010.2:c.2445C= XP_011526312.1:p.Asn815=
XR_001753685.2:n.2857C=
XR_001753686.2:n.2500C=
NM_000527.5:c.2523C= MANE Select NP_000518.1:p.Asn841=
NM_001195798.2:c.2523C= NP_001182727.1:p.Asn841=
NM_001195799.2:c.2400C= NP_001182728.1:p.Asn800=
NM_001195800.2:c.2019C= NP_001182729.1:p.Asn673=
NM_001195803.2:c.1989C= NP_001182732.1:p.Asn663=