Canonical Allele Identifier: CA2322779619
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128178C= , CM000681.2:g.11128178C= GRCh38
NC_000019.9:g.11238854C= , CM000681.1:g.11238854C= GRCh37
NC_000019.8:g.11099854C= NCBI36
NG_009060.1:g.43798C= , LRG_274:g.43798C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2647+93C= ENSP00000252444.6:n.2647+93C=
ENST00000559340.2:c.*458+93C= ENSP00000453696.2:n.*458+93C=
ENST00000560467.2:c.2269+93C= ENSP00000453513.2:n.2269+93C=
ENST00000558518.6:c.2389+93C= MANE Select ENSP00000454071.1:n.2389+93C=
ENST00000252444.9:c.2643+93C=
ENST00000455727.6:c.1885+93C= ENSP00000397829.2:n.1885+93C=
ENST00000535915.5:c.2266+93C= ENSP00000440520.1:n.2266+93C=
ENST00000545707.5:c.1855+93C= ENSP00000437639.1:n.1855+93C=
ENST00000557933.5:c.2389+93C= ENSP00000453557.1:n.2389+93C=
ENST00000558013.5:c.2389+93C= ENSP00000453346.1:n.2389+93C=
ENST00000558518.5:c.2389+93C= ENSP00000454071.1:n.2389+93C=
ENST00000560628.1:n.108+524C=
NM_000527.4:c.2389+93C= , LRG_274t1:c.2389+93C= NP_000518.1:n.2389+93C=
NM_001195798.1:c.2389+93C= NP_001182727.1:n.2389+93C=
NM_001195799.1:c.2266+93C= NP_001182728.1:n.2266+93C=
NM_001195800.1:c.1885+93C= NP_001182729.1:n.1885+93C=
NM_001195803.1:c.1855+93C= NP_001182732.1:n.1855+93C=
XM_011528010.1:c.2312-1335C= XP_011526312.1:n.2312-1335C=
XM_011528011.1:c.2008+93C= XP_011526313.1:n.2008+93C=
XR_244074.2:n.2399+93C=
XM_011528010.2:c.2312-1335C= XP_011526312.1:n.2312-1335C=
XR_001753685.2:n.2723+93C=
XR_001753686.2:n.2366+93C=
NM_000527.5:c.2389+93C= MANE Select NP_000518.1:n.2389+93C=
NM_001195798.2:c.2389+93C= NP_001182727.1:n.2389+93C=
NM_001195799.2:c.2266+93C= NP_001182728.1:n.2266+93C=
NM_001195800.2:c.1885+93C= NP_001182729.1:n.1885+93C=
NM_001195803.2:c.1855+93C= NP_001182732.1:n.1855+93C=