Canonical Allele Identifier: CA2322779598
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128123C= , CM000681.2:g.11128123C= GRCh38
NC_000019.9:g.11238799C= , CM000681.1:g.11238799C= GRCh37
NC_000019.8:g.11099799C= NCBI36
NG_009060.1:g.43743C= , LRG_274:g.43743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2647+38C= ENSP00000252444.6:n.2647+38C=
ENST00000559340.2:c.*458+38C= ENSP00000453696.2:n.*458+38C=
ENST00000560467.2:c.2269+38C= ENSP00000453513.2:n.2269+38C=
ENST00000558518.6:c.2389+38C= MANE Select ENSP00000454071.1:n.2389+38C=
ENST00000252444.9:c.2643+38C=
ENST00000455727.6:c.1885+38C= ENSP00000397829.2:n.1885+38C=
ENST00000535915.5:c.2266+38C= ENSP00000440520.1:n.2266+38C=
ENST00000545707.5:c.1855+38C= ENSP00000437639.1:n.1855+38C=
ENST00000557933.5:c.2389+38C= ENSP00000453557.1:n.2389+38C=
ENST00000558013.5:c.2389+38C= ENSP00000453346.1:n.2389+38C=
ENST00000558518.5:c.2389+38C= ENSP00000454071.1:n.2389+38C=
ENST00000560628.1:n.108+469C=
NM_000527.4:c.2389+38C= , LRG_274t1:c.2389+38C= NP_000518.1:n.2389+38C=
NM_001195798.1:c.2389+38C= NP_001182727.1:n.2389+38C=
NM_001195799.1:c.2266+38C= NP_001182728.1:n.2266+38C=
NM_001195800.1:c.1885+38C= NP_001182729.1:n.1885+38C=
NM_001195803.1:c.1855+38C= NP_001182732.1:n.1855+38C=
XM_011528010.1:c.2312-1390C= XP_011526312.1:n.2312-1390C=
XM_011528011.1:c.2008+38C= XP_011526313.1:n.2008+38C=
XR_244074.2:n.2399+38C=
XM_011528010.2:c.2312-1390C= XP_011526312.1:n.2312-1390C=
XR_001753685.2:n.2723+38C=
XR_001753686.2:n.2366+38C=
NM_000527.5:c.2389+38C= MANE Select NP_000518.1:n.2389+38C=
NM_001195798.2:c.2389+38C= NP_001182727.1:n.2389+38C=
NM_001195799.2:c.2266+38C= NP_001182728.1:n.2266+38C=
NM_001195800.2:c.1885+38C= NP_001182729.1:n.1885+38C=
NM_001195803.2:c.1855+38C= NP_001182732.1:n.1855+38C=