Canonical Allele Identifier: CA404085260
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113424G>A , CM000681.2:g.11113424G>A GRCh38
NC_000019.9:g.11224100G>A , CM000681.1:g.11224100G>A GRCh37
NC_000019.8:g.11085100G>A NCBI36
NG_009060.1:g.29044G>A , LRG_274:g.29044G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1591G>A ENSP00000252444.6:p.Asp531Asn
ENST00000559340.2:c.1333G>A ENSP00000453696.2:p.Asp445Asn
ENST00000560467.2:c.1213G>A ENSP00000453513.2:p.Asp405Asn
ENST00000558518.6:c.1333G>A MANE Select ENSP00000454071.1:p.Asp445Asn
ENST00000252444.9:c.1587G>A
ENST00000455727.6:c.829G>A ENSP00000397829.2:p.Asp277Asn
ENST00000535915.5:c.1210G>A ENSP00000440520.1:p.Asp404Asn
ENST00000545707.5:c.952G>A ENSP00000437639.1:p.Asp318Asn
ENST00000557933.5:c.1333G>A ENSP00000453557.1:p.Asp445Asn
ENST00000558013.5:c.1333G>A ENSP00000453346.1:p.Asp445Asn
ENST00000558518.5:c.1333G>A ENSP00000454071.1:p.Asp445Asn
ENST00000559340.1:c.54G>A
ENST00000560173.1:n.332G>A
ENST00000560467.1:c.813G>A
NM_000527.4:c.1333G>A , LRG_274t1:c.1333G>A NP_000518.1:p.Asp445Asn
NM_001195798.1:c.1333G>A NP_001182727.1:p.Asp445Asn
NM_001195799.1:c.1210G>A NP_001182728.1:p.Asp404Asn
NM_001195800.1:c.829G>A NP_001182729.1:p.Asp277Asn
NM_001195803.1:c.952G>A NP_001182732.1:p.Asp318Asn
XM_011528010.1:c.1333G>A XP_011526312.1:p.Asp445Asn
XM_011528011.1:c.952G>A XP_011526313.1:p.Asp318Asn
XR_244074.2:n.1483G>A
XM_011528010.2:c.1333G>A XP_011526312.1:p.Asp445Asn
XR_001753685.2:n.1450G>A
XR_001753686.2:n.1450G>A
NM_000527.5:c.1333G>A MANE Select NP_000518.1:p.Asp445Asn
NM_001195798.2:c.1333G>A NP_001182727.1:p.Asp445Asn
NM_001195799.2:c.1210G>A NP_001182728.1:p.Asp404Asn
NM_001195800.2:c.829G>A NP_001182729.1:p.Asp277Asn
NM_001195803.2:c.952G>A NP_001182732.1:p.Asp318Asn