Canonical Allele Identifier: CA783244327
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs1303154907

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107263del , CM000681.2:g.11107263del GRCh38
NC_000019.9:g.11217939del , CM000681.1:g.11217939del GRCh37
NC_000019.8:g.11078939del NCBI36
NG_009060.1:g.22883del , LRG_274:g.22883del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1076-129del ENSP00000252444.6:n.1076-129del
ENST00000559340.2:c.818-129del ENSP00000453696.2:n.818-129del
ENST00000560467.2:c.818-129del ENSP00000453513.2:n.818-129del
ENST00000558518.6:c.818-129del MANE Select ENSP00000454071.1:n.818-129del
ENST00000252444.9:c.1072-129del
ENST00000455727.6:c.314-129del ENSP00000397829.2:n.314-129del
ENST00000535915.5:c.695-129del ENSP00000440520.1:n.695-129del
ENST00000545707.5:c.437-129del ENSP00000437639.1:n.437-129del
ENST00000557933.5:c.818-129del ENSP00000453557.1:n.818-129del
ENST00000558013.5:c.818-129del ENSP00000453346.1:n.818-129del
ENST00000558518.5:c.818-129del ENSP00000454071.1:n.818-129del
ENST00000558528.1:n.333-129del
ENST00000560467.1:c.418-129del
NM_000527.4:c.818-129del , LRG_274t1:c.818-129del NP_000518.1:n.818-129del
NM_001195798.1:c.818-129del NP_001182727.1:n.818-129del
NM_001195799.1:c.695-129del NP_001182728.1:n.695-129del
NM_001195800.1:c.314-129del NP_001182729.1:n.314-129del
NM_001195803.1:c.437-129del NP_001182732.1:n.437-129del
XM_011528010.1:c.818-129del XP_011526312.1:n.818-129del
XM_011528011.1:c.437-129del XP_011526313.1:n.437-129del
XR_244074.2:n.968-129del
XM_011528010.2:c.818-129del XP_011526312.1:n.818-129del
XR_001753685.2:n.935-129del
XR_001753686.2:n.935-129del
NM_000527.5:c.818-129del MANE Select NP_000518.1:n.818-129del
NM_001195798.2:c.818-129del NP_001182727.1:n.818-129del
NM_001195799.2:c.695-129del NP_001182728.1:n.695-129del
NM_001195800.2:c.314-129del NP_001182729.1:n.314-129del
NM_001195803.2:c.437-129del NP_001182732.1:n.437-129del