Canonical Allele Identifier: CA2322779583
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128104C= , CM000681.2:g.11128104C= GRCh38
NC_000019.9:g.11238780C= , CM000681.1:g.11238780C= GRCh37
NC_000019.8:g.11099780C= NCBI36
NG_009060.1:g.43724C= , LRG_274:g.43724C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2647+19C= ENSP00000252444.6:n.2647+19C=
ENST00000559340.2:c.*458+19C= ENSP00000453696.2:n.*458+19C=
ENST00000560467.2:c.2269+19C= ENSP00000453513.2:n.2269+19C=
ENST00000558518.6:c.2389+19C= MANE Select ENSP00000454071.1:n.2389+19C=
ENST00000252444.9:c.2643+19C=
ENST00000455727.6:c.1885+19C= ENSP00000397829.2:n.1885+19C=
ENST00000535915.5:c.2266+19C= ENSP00000440520.1:n.2266+19C=
ENST00000545707.5:c.1855+19C= ENSP00000437639.1:n.1855+19C=
ENST00000557933.5:c.2389+19C= ENSP00000453557.1:n.2389+19C=
ENST00000558013.5:c.2389+19C= ENSP00000453346.1:n.2389+19C=
ENST00000558518.5:c.2389+19C= ENSP00000454071.1:n.2389+19C=
ENST00000560628.1:n.108+450C=
NM_000527.4:c.2389+19C= , LRG_274t1:c.2389+19C= NP_000518.1:n.2389+19C=
NM_001195798.1:c.2389+19C= NP_001182727.1:n.2389+19C=
NM_001195799.1:c.2266+19C= NP_001182728.1:n.2266+19C=
NM_001195800.1:c.1885+19C= NP_001182729.1:n.1885+19C=
NM_001195803.1:c.1855+19C= NP_001182732.1:n.1855+19C=
XM_011528010.1:c.2312-1409C= XP_011526312.1:n.2312-1409C=
XM_011528011.1:c.2008+19C= XP_011526313.1:n.2008+19C=
XR_244074.2:n.2399+19C=
XM_011528010.2:c.2312-1409C= XP_011526312.1:n.2312-1409C=
XR_001753685.2:n.2723+19C=
XR_001753686.2:n.2366+19C=
NM_000527.5:c.2389+19C= MANE Select NP_000518.1:n.2389+19C=
NM_001195798.2:c.2389+19C= NP_001182727.1:n.2389+19C=
NM_001195799.2:c.2266+19C= NP_001182728.1:n.2266+19C=
NM_001195800.2:c.1885+19C= NP_001182729.1:n.1885+19C=
NM_001195803.2:c.1855+19C= NP_001182732.1:n.1855+19C=