Canonical Allele Identifier: CA404093870
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120469G>C , CM000681.2:g.11120469G>C GRCh38
NC_000019.9:g.11231145G>C , CM000681.1:g.11231145G>C GRCh37
NC_000019.8:g.11092145G>C NCBI36
NG_009060.1:g.36089G>C , LRG_274:g.36089G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2345G>C ENSP00000252444.6:p.Cys782Ser
ENST00000559340.2:c.*156G>C ENSP00000453696.2:n.*156G>C
ENST00000560467.2:c.1967G>C ENSP00000453513.2:p.Cys656Ser
ENST00000558518.6:c.2087G>C MANE Select ENSP00000454071.1:p.Cys696Ser
ENST00000252444.9:c.2341G>C
ENST00000455727.6:c.1583G>C ENSP00000397829.2:p.Cys528Ser
ENST00000535915.5:c.1964G>C ENSP00000440520.1:p.Cys655Ser
ENST00000545707.5:c.1606+236G>C ENSP00000437639.1:n.1606+236G>C
ENST00000557933.5:c.2087G>C ENSP00000453557.1:p.Cys696Ser
ENST00000558013.5:c.2087G>C ENSP00000453346.1:p.Cys696Ser
ENST00000558518.5:c.2087G>C ENSP00000454071.1:p.Cys696Ser
NM_000527.4:c.2087G>C , LRG_274t1:c.2087G>C NP_000518.1:p.Cys696Ser
NM_001195798.1:c.2087G>C NP_001182727.1:p.Cys696Ser
NM_001195799.1:c.1964G>C NP_001182728.1:p.Cys655Ser
NM_001195800.1:c.1583G>C NP_001182729.1:p.Cys528Ser
NM_001195803.1:c.1606+236G>C NP_001182732.1:n.1606+236G>C
XM_011528010.1:c.2087G>C XP_011526312.1:p.Cys696Ser
XM_011528011.1:c.1706G>C XP_011526313.1:p.Cys569Ser
XR_244074.2:n.2097G>C
XM_011528010.2:c.2087G>C XP_011526312.1:p.Cys696Ser
XR_001753685.2:n.2204G>C
XR_001753686.2:n.2064G>C
NM_000527.5:c.2087G>C MANE Select NP_000518.1:p.Cys696Ser
NM_001195798.2:c.2087G>C NP_001182727.1:p.Cys696Ser
NM_001195799.2:c.1964G>C NP_001182728.1:p.Cys655Ser
NM_001195800.2:c.1583G>C NP_001182729.1:p.Cys528Ser
NM_001195803.2:c.1606+236G>C NP_001182732.1:n.1606+236G>C