Canonical Allele Identifier: CA2582473475
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11105658dup , CM000681.2:g.11105658dup GRCh38
NC_000019.9:g.11216334dup , CM000681.1:g.11216334dup GRCh37
NC_000019.8:g.11077334dup NCBI36
NG_009060.1:g.21278dup , LRG_274:g.21278dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.952+58dup ENSP00000252444.6:n.952+58dup
ENST00000559340.2:c.694+58dup ENSP00000453696.2:n.694+58dup
ENST00000560467.2:c.694+58dup ENSP00000453513.2:n.694+58dup
ENST00000558518.6:c.694+58dup MANE Select ENSP00000454071.1:n.694+58dup
ENST00000252444.9:c.948+58dup
ENST00000455727.6:c.314-1734dup ENSP00000397829.2:n.314-1734dup
ENST00000535915.5:c.571+58dup ENSP00000440520.1:n.571+58dup
ENST00000545707.5:c.314-907dup ENSP00000437639.1:n.314-907dup
ENST00000557933.5:c.694+58dup ENSP00000453557.1:n.694+58dup
ENST00000558013.5:c.694+58dup ENSP00000453346.1:n.694+58dup
ENST00000558518.5:c.694+58dup ENSP00000454071.1:n.694+58dup
ENST00000560467.1:c.294+58dup
NM_000527.4:c.694+58dup , LRG_274t1:c.694+58dup NP_000518.1:n.694+58dup
NM_001195798.1:c.694+58dup NP_001182727.1:n.694+58dup
NM_001195799.1:c.571+58dup NP_001182728.1:n.571+58dup
NM_001195800.1:c.314-1734dup NP_001182729.1:n.314-1734dup
NM_001195803.1:c.314-907dup NP_001182732.1:n.314-907dup
XM_011528010.1:c.694+58dup XP_011526312.1:n.694+58dup
XM_011528011.1:c.314-907dup XP_011526313.1:n.314-907dup
XR_244074.2:n.844+58dup
XM_011528010.2:c.694+58dup XP_011526312.1:n.694+58dup
XR_001753685.2:n.811+58dup
XR_001753686.2:n.811+58dup
NM_000527.5:c.694+58dup MANE Select NP_000518.1:n.694+58dup
NM_001195798.2:c.694+58dup NP_001182727.1:n.694+58dup
NM_001195799.2:c.571+58dup NP_001182728.1:n.571+58dup
NM_001195800.2:c.314-1734dup NP_001182729.1:n.314-1734dup
NM_001195803.2:c.314-907dup NP_001182732.1:n.314-907dup