Canonical Allele Identifier: CA645373250
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 430747
ClinVar RCV Id: RCV000495900

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11100333del , CM000681.2:g.11100333del GRCh38
NC_000019.9:g.11211009del , CM000681.1:g.11211009del GRCh37
NC_000019.8:g.11072009del NCBI36
NG_009060.1:g.15953del , LRG_274:g.15953del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.436del ENSP00000252444.6:p.Gln146ArgfsTer?
ENST00000559340.2:c.178del ENSP00000453696.2:p.Gln60ArgfsTer?
ENST00000560467.2:c.178del ENSP00000453513.2:p.Gln60ArgfsTer?
ENST00000558518.6:c.178del MANE Select ENSP00000454071.1:p.Gln60ArgfsTer?
ENST00000252444.9:c.432del
ENST00000455727.6:c.178del ENSP00000397829.2:p.Gln60ArgfsTer?
ENST00000535915.5:c.178del ENSP00000440520.1:p.Gln60ArgfsTer?
ENST00000545707.5:c.178del ENSP00000437639.1:p.Gln60ArgfsTer?
ENST00000557933.5:c.178del ENSP00000453557.1:p.Gln60ArgfsTer?
ENST00000557958.1:n.264del
ENST00000558013.5:c.178del ENSP00000453346.1:p.Gln60ArgfsTer?
ENST00000558518.5:c.178del ENSP00000454071.1:p.Gln60ArgfsTer?
ENST00000560502.5:n.264del
NM_000527.4:c.178del , LRG_274t1:c.178del NP_000518.1:p.Gln60ArgfsTer?
NM_001195798.1:c.178del NP_001182727.1:p.Gln60ArgfsTer?
NM_001195799.1:c.178del NP_001182728.1:p.Gln60ArgfsTer?
NM_001195800.1:c.178del NP_001182729.1:p.Gln60ArgfsTer?
NM_001195803.1:c.178del NP_001182732.1:p.Gln60ArgfsTer?
XM_011528010.1:c.178del XP_011526312.1:p.Gln60ArgfsTer?
XM_011528011.1:c.178del XP_011526313.1:p.Gln60ArgfsTer?
XR_244074.2:n.328del
XM_011528010.2:c.178del XP_011526312.1:p.Gln60ArgfsTer?
XR_001753685.2:n.295del
XR_001753686.2:n.295del
NM_000527.5:c.178del MANE Select NP_000518.1:p.Gln60ArgfsTer?
NM_001195798.2:c.178del NP_001182727.1:p.Gln60ArgfsTer?
NM_001195799.2:c.178del NP_001182728.1:p.Gln60ArgfsTer?
NM_001195800.2:c.178del NP_001182729.1:p.Gln60ArgfsTer?
NM_001195803.2:c.178del NP_001182732.1:p.Gln60ArgfsTer?