Canonical Allele Identifier: CA1139666261
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 947606
ClinVar RCV Id: RCV001218715
dbSNP Id: rs2077313046

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107457del , CM000681.2:g.11107457del GRCh38
NC_000019.9:g.11218133del , CM000681.1:g.11218133del GRCh37
NC_000019.8:g.11079133del NCBI36
NG_009060.1:g.23077del , LRG_274:g.23077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1141del ENSP00000252444.6:p.Val381SerfsTer?
ENST00000559340.2:c.883del ENSP00000453696.2:p.Val295SerfsTer?
ENST00000560467.2:c.883del ENSP00000453513.2:p.Val295SerfsTer?
ENST00000558518.6:c.883del MANE Select ENSP00000454071.1:p.Val295SerfsTer?
ENST00000252444.9:c.1137del
ENST00000455727.6:c.379del ENSP00000397829.2:p.Val127SerfsTer?
ENST00000535915.5:c.760del ENSP00000440520.1:p.Val254SerfsTer?
ENST00000545707.5:c.502del ENSP00000437639.1:p.Val168SerfsTer?
ENST00000557933.5:c.883del ENSP00000453557.1:p.Val295SerfsTer?
ENST00000558013.5:c.883del ENSP00000453346.1:p.Val295SerfsTer?
ENST00000558518.5:c.883del ENSP00000454071.1:p.Val295SerfsTer?
ENST00000558528.1:n.398del
ENST00000560467.1:c.483del
NM_000527.4:c.883del , LRG_274t1:c.883del NP_000518.1:p.Val295SerfsTer?
NM_001195798.1:c.883del NP_001182727.1:p.Val295SerfsTer?
NM_001195799.1:c.760del NP_001182728.1:p.Val254SerfsTer?
NM_001195800.1:c.379del NP_001182729.1:p.Val127SerfsTer?
NM_001195803.1:c.502del NP_001182732.1:p.Val168SerfsTer?
XM_011528010.1:c.883del XP_011526312.1:p.Val295SerfsTer?
XM_011528011.1:c.502del XP_011526313.1:p.Val168SerfsTer?
XR_244074.2:n.1033del
XM_011528010.2:c.883del XP_011526312.1:p.Val295SerfsTer?
XR_001753685.2:n.1000del
XR_001753686.2:n.1000del
NM_000527.5:c.883del MANE Select NP_000518.1:p.Val295SerfsTer?
NM_001195798.2:c.883del NP_001182727.1:p.Val295SerfsTer?
NM_001195799.2:c.760del NP_001182728.1:p.Val254SerfsTer?
NM_001195800.2:c.379del NP_001182729.1:p.Val127SerfsTer?
NM_001195803.2:c.502del NP_001182732.1:p.Val168SerfsTer?