Canonical Allele Identifier: CA2497030087
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116879del , CM000681.2:g.11116879del GRCh38
NC_000019.9:g.11227555del , CM000681.1:g.11227555del GRCh37
NC_000019.8:g.11088555del NCBI36
NG_009060.1:g.32499del , LRG_274:g.32499del

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1984del ENSP00000252444.6:p.Tyr662ThrfsTer?
ENST00000559340.2:c.1705+667del ENSP00000453696.2:n.1705+667del
ENST00000560467.2:c.1606del ENSP00000453513.2:p.Tyr536ThrfsTer?
ENST00000558518.6:c.1726del MANE Select ENSP00000454071.1:p.Tyr576ThrfsTer?
ENST00000252444.9:c.1980del
ENST00000455727.6:c.1222del ENSP00000397829.2:p.Tyr408ThrfsTer?
ENST00000535915.5:c.1603del ENSP00000440520.1:p.Tyr535ThrfsTer?
ENST00000545707.5:c.1345del ENSP00000437639.1:p.Tyr449ThrfsTer?
ENST00000557933.5:c.1726del ENSP00000453557.1:p.Tyr576ThrfsTer?
ENST00000558013.5:c.1726del ENSP00000453346.1:p.Tyr576ThrfsTer?
ENST00000558518.5:c.1726del ENSP00000454071.1:p.Tyr576ThrfsTer?
ENST00000559340.1:c.426+667del
NM_000527.4:c.1726del , LRG_274t1:c.1726del NP_000518.1:p.Tyr576ThrfsTer?
NM_001195798.1:c.1726del NP_001182727.1:p.Tyr576ThrfsTer?
NM_001195799.1:c.1603del NP_001182728.1:p.Tyr535ThrfsTer?
NM_001195800.1:c.1222del NP_001182729.1:p.Tyr408ThrfsTer?
NM_001195803.1:c.1345del NP_001182732.1:p.Tyr449ThrfsTer?
XM_011528010.1:c.1726del XP_011526312.1:p.Tyr576ThrfsTer?
XM_011528011.1:c.1345del XP_011526313.1:p.Tyr449ThrfsTer?
XR_244074.2:n.1855+667del
XM_011528010.2:c.1726del XP_011526312.1:p.Tyr576ThrfsTer?
XR_001753685.2:n.1843del
XR_001753686.2:n.1822+667del
NM_000527.5:c.1726del MANE Select NP_000518.1:p.Tyr576ThrfsTer?
NM_001195798.2:c.1726del NP_001182727.1:p.Tyr576ThrfsTer?
NM_001195799.2:c.1603del NP_001182728.1:p.Tyr535ThrfsTer?
NM_001195800.2:c.1222del NP_001182729.1:p.Tyr408ThrfsTer?
NM_001195803.2:c.1345del NP_001182732.1:p.Tyr449ThrfsTer?