Canonical Allele Identifier: CA404086121
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113627T>C , CM000681.2:g.11113627T>C GRCh38
NC_000019.9:g.11224303T>C , CM000681.1:g.11224303T>C GRCh37
NC_000019.8:g.11085303T>C NCBI36
NG_009060.1:g.29247T>C , LRG_274:g.29247T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1709T>C ENSP00000252444.6:p.Ile570Thr
ENST00000559340.2:c.1451T>C ENSP00000453696.2:p.Ile484Thr
ENST00000560467.2:c.1331T>C ENSP00000453513.2:p.Ile444Thr
ENST00000558518.6:c.1451T>C MANE Select ENSP00000454071.1:p.Ile484Thr
ENST00000252444.9:c.1705T>C
ENST00000455727.6:c.947T>C ENSP00000397829.2:p.Ile316Thr
ENST00000535915.5:c.1328T>C ENSP00000440520.1:p.Ile443Thr
ENST00000545707.5:c.1070T>C ENSP00000437639.1:p.Ile357Thr
ENST00000557933.5:c.1451T>C ENSP00000453557.1:p.Ile484Thr
ENST00000558013.5:c.1451T>C ENSP00000453346.1:p.Ile484Thr
ENST00000558518.5:c.1451T>C ENSP00000454071.1:p.Ile484Thr
ENST00000559340.1:c.172T>C
NM_000527.4:c.1451T>C , LRG_274t1:c.1451T>C NP_000518.1:p.Ile484Thr
NM_001195798.1:c.1451T>C NP_001182727.1:p.Ile484Thr
NM_001195799.1:c.1328T>C NP_001182728.1:p.Ile443Thr
NM_001195800.1:c.947T>C NP_001182729.1:p.Ile316Thr
NM_001195803.1:c.1070T>C NP_001182732.1:p.Ile357Thr
XM_011528010.1:c.1451T>C XP_011526312.1:p.Ile484Thr
XM_011528011.1:c.1070T>C XP_011526313.1:p.Ile357Thr
XR_244074.2:n.1601T>C
XM_011528010.2:c.1451T>C XP_011526312.1:p.Ile484Thr
XR_001753685.2:n.1568T>C
XR_001753686.2:n.1568T>C
NM_000527.5:c.1451T>C MANE Select NP_000518.1:p.Ile484Thr
NM_001195798.2:c.1451T>C NP_001182727.1:p.Ile484Thr
NM_001195799.2:c.1328T>C NP_001182728.1:p.Ile443Thr
NM_001195800.2:c.947T>C NP_001182729.1:p.Ile316Thr
NM_001195803.2:c.1070T>C NP_001182732.1:p.Ile357Thr