Canonical Allele Identifier: CA404093498
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120394C>A , CM000681.2:g.11120394C>A GRCh38
NC_000019.9:g.11231070C>A , CM000681.1:g.11231070C>A GRCh37
NC_000019.8:g.11092070C>A NCBI36
NG_009060.1:g.36014C>A , LRG_274:g.36014C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2270C>A ENSP00000252444.6:p.Thr757Asn
ENST00000559340.2:c.*81C>A ENSP00000453696.2:n.*81C>A
ENST00000560467.2:c.1892C>A ENSP00000453513.2:p.Thr631Asn
ENST00000558518.6:c.2012C>A MANE Select ENSP00000454071.1:p.Thr671Asn
ENST00000252444.9:c.2266C>A
ENST00000455727.6:c.1508C>A ENSP00000397829.2:p.Thr503Asn
ENST00000535915.5:c.1889C>A ENSP00000440520.1:p.Thr630Asn
ENST00000545707.5:c.1606+161C>A ENSP00000437639.1:n.1606+161C>A
ENST00000557933.5:c.2012C>A ENSP00000453557.1:p.Thr671Asn
ENST00000558013.5:c.2012C>A ENSP00000453346.1:p.Thr671Asn
ENST00000558518.5:c.2012C>A ENSP00000454071.1:p.Thr671Asn
ENST00000559340.1:c.593C>A
NM_000527.4:c.2012C>A , LRG_274t1:c.2012C>A NP_000518.1:p.Thr671Asn
NM_001195798.1:c.2012C>A NP_001182727.1:p.Thr671Asn
NM_001195799.1:c.1889C>A NP_001182728.1:p.Thr630Asn
NM_001195800.1:c.1508C>A NP_001182729.1:p.Thr503Asn
NM_001195803.1:c.1606+161C>A NP_001182732.1:n.1606+161C>A
XM_011528010.1:c.2012C>A XP_011526312.1:p.Thr671Asn
XM_011528011.1:c.1631C>A XP_011526313.1:p.Thr544Asn
XR_244074.2:n.2022C>A
XM_011528010.2:c.2012C>A XP_011526312.1:p.Thr671Asn
XR_001753685.2:n.2129C>A
XR_001753686.2:n.1989C>A
NM_000527.5:c.2012C>A MANE Select NP_000518.1:p.Thr671Asn
NM_001195798.2:c.2012C>A NP_001182727.1:p.Thr671Asn
NM_001195799.2:c.1889C>A NP_001182728.1:p.Thr630Asn
NM_001195800.2:c.1508C>A NP_001182729.1:p.Thr503Asn
NM_001195803.2:c.1606+161C>A NP_001182732.1:n.1606+161C>A