Canonical Allele Identifier: CA2955303476
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107444dup , CM000681.2:g.11107444dup GRCh38
NC_000019.9:g.11218120dup , CM000681.1:g.11218120dup GRCh37
NC_000019.8:g.11079120dup NCBI36
NG_009060.1:g.23064dup , LRG_274:g.23064dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1128dup ENSP00000252444.6:p.Thr377HisfsTer10
ENST00000559340.2:c.870dup ENSP00000453696.2:p.Thr291HisfsTer10
ENST00000560467.2:c.870dup ENSP00000453513.2:p.Thr291HisfsTer10
ENST00000558518.6:c.870dup MANE Select ENSP00000454071.1:p.Thr291HisfsTer10
ENST00000252444.9:c.1124dup
ENST00000455727.6:c.366dup ENSP00000397829.2:p.Thr123HisfsTer10
ENST00000535915.5:c.747dup ENSP00000440520.1:p.Thr250HisfsTer10
ENST00000545707.5:c.489dup ENSP00000437639.1:p.Thr164HisfsTer10
ENST00000557933.5:c.870dup ENSP00000453557.1:p.Thr291HisfsTer10
ENST00000558013.5:c.870dup ENSP00000453346.1:p.Thr291HisfsTer10
ENST00000558518.5:c.870dup ENSP00000454071.1:p.Thr291HisfsTer10
ENST00000558528.1:n.385dup
ENST00000560467.1:c.470dup
NM_000527.4:c.870dup , LRG_274t1:c.870dup NP_000518.1:p.Thr291HisfsTer10
NM_001195798.1:c.870dup NP_001182727.1:p.Thr291HisfsTer10
NM_001195799.1:c.747dup NP_001182728.1:p.Thr250HisfsTer10
NM_001195800.1:c.366dup NP_001182729.1:p.Thr123HisfsTer10
NM_001195803.1:c.489dup NP_001182732.1:p.Thr164HisfsTer10
XM_011528010.1:c.870dup XP_011526312.1:p.Thr291HisfsTer10
XM_011528011.1:c.489dup XP_011526313.1:p.Thr164HisfsTer10
XR_244074.2:n.1020dup
XM_011528010.2:c.870dup XP_011526312.1:p.Thr291HisfsTer10
XR_001753685.2:n.987dup
XR_001753686.2:n.987dup
NM_000527.5:c.870dup MANE Select NP_000518.1:p.Thr291HisfsTer10
NM_001195798.2:c.870dup NP_001182727.1:p.Thr291HisfsTer10
NM_001195799.2:c.747dup NP_001182728.1:p.Thr250HisfsTer10
NM_001195800.2:c.366dup NP_001182729.1:p.Thr123HisfsTer10
NM_001195803.2:c.489dup NP_001182732.1:p.Thr164HisfsTer10