Canonical Allele Identifier: CA993517458
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs2077442636

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11114977_11114980del , CM000681.2:g.11114977_11114980del GRCh38
NC_000019.9:g.11225653_11225656del , CM000681.1:g.11225653_11225656del GRCh37
NC_000019.8:g.11086653_11086656del NCBI36
NG_009060.1:g.30597_30600del , LRG_274:g.30597_30600del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1845-1117_1845-1114del ENSP00000252444.6:n.1845-1117_1845-1114del
ENST00000559340.2:c.1587-1117_1587-1114del ENSP00000453696.2:n.1587-1117_1587-1114del
ENST00000560467.2:c.1467-1117_1467-1114del ENSP00000453513.2:n.1467-1117_1467-1114del
ENST00000558518.6:c.1587-1117_1587-1114del MANE Select ENSP00000454071.1:n.1587-1117_1587-1114del
ENST00000252444.9:c.1841-1117_1841-1114del
ENST00000455727.6:c.1083-1117_1083-1114del ENSP00000397829.2:n.1083-1117_1083-1114del
ENST00000535915.5:c.1464-1117_1464-1114del ENSP00000440520.1:n.1464-1117_1464-1114del
ENST00000545707.5:c.1206-1117_1206-1114del ENSP00000437639.1:n.1206-1117_1206-1114del
ENST00000557933.5:c.1587-1117_1587-1114del ENSP00000453557.1:n.1587-1117_1587-1114del
ENST00000558013.5:c.1587-1117_1587-1114del ENSP00000453346.1:n.1587-1117_1587-1114del
ENST00000558518.5:c.1587-1117_1587-1114del ENSP00000454071.1:n.1587-1117_1587-1114del
ENST00000559340.1:c.308-1117_308-1114del
NM_000527.4:c.1587-1117_1587-1114del , LRG_274t1:c.1587-1117_1587-1114del NP_000518.1:n.1587-1117_1587-1114del
NM_001195798.1:c.1587-1117_1587-1114del NP_001182727.1:n.1587-1117_1587-1114del
NM_001195799.1:c.1464-1117_1464-1114del NP_001182728.1:n.1464-1117_1464-1114del
NM_001195800.1:c.1083-1117_1083-1114del NP_001182729.1:n.1083-1117_1083-1114del
NM_001195803.1:c.1206-1117_1206-1114del NP_001182732.1:n.1206-1117_1206-1114del
XM_011528010.1:c.1587-1117_1587-1114del XP_011526312.1:n.1587-1117_1587-1114del
XM_011528011.1:c.1206-1117_1206-1114del XP_011526313.1:n.1206-1117_1206-1114del
XR_244074.2:n.1737-1117_1737-1114del
XM_011528010.2:c.1587-1117_1587-1114del XP_011526312.1:n.1587-1117_1587-1114del
XR_001753685.2:n.1704-1117_1704-1114del
XR_001753686.2:n.1704-1117_1704-1114del
NM_000527.5:c.1587-1117_1587-1114del MANE Select NP_000518.1:n.1587-1117_1587-1114del
NM_001195798.2:c.1587-1117_1587-1114del NP_001182727.1:n.1587-1117_1587-1114del
NM_001195799.2:c.1464-1117_1464-1114del NP_001182728.1:n.1464-1117_1464-1114del
NM_001195800.2:c.1083-1117_1083-1114del NP_001182729.1:n.1083-1117_1083-1114del
NM_001195803.2:c.1206-1117_1206-1114del NP_001182732.1:n.1206-1117_1206-1114del