Canonical Allele Identifier: CA2322775561
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120410_11120422delinsCTGCCAGTATCTG , CM000681.2:g.11120410_11120422delinsCTGCCAGTATCTG GRCh38
NC_000019.9:g.11231086_11231098delinsCTGCCAGTATCTG , CM000681.1:g.11231086_11231098delinsCTGCCAGTATCTG GRCh37
NC_000019.8:g.11092086_11092098delinsCTGCCAGTATCTG NCBI36
NG_009060.1:g.36030_36042delinsCTGCCAGTATCTG , LRG_274:g.36030_36042delinsCTGCCAGTATCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2286_2298delinsCTGCCAGTATCTG ENSP00000252444.6:p.Gly762=
ENST00000559340.2:c.*97_*109delinsCTGCCAGTATCTG ENSP00000453696.2:n.*97_*109delinsCTGCCAGTATCTG
ENST00000560467.2:c.1908_1920delinsCTGCCAGTATCTG ENSP00000453513.2:p.Gly636=
ENST00000558518.6:c.2028_2040delinsCTGCCAGTATCTG MANE Select ENSP00000454071.1:p.Gly676=
ENST00000252444.9:c.2282_2294delinsCTGCCAGTATCTG
ENST00000455727.6:c.1524_1536delinsCTGCCAGTATCTG ENSP00000397829.2:p.Gly508=
ENST00000535915.5:c.1905_1917delinsCTGCCAGTATCTG ENSP00000440520.1:p.Gly635=
ENST00000545707.5:c.1606+177_1606+189delinsCTGCCAGTATCTG ENSP00000437639.1:n.1606+177_1606+189delinsCTGCCAGTATCTG
ENST00000557933.5:c.2028_2040delinsCTGCCAGTATCTG ENSP00000453557.1:p.Gly676=
ENST00000558013.5:c.2028_2040delinsCTGCCAGTATCTG ENSP00000453346.1:p.Gly676=
ENST00000558518.5:c.2028_2040delinsCTGCCAGTATCTG ENSP00000454071.1:p.Gly676=
NM_000527.4:c.2028_2040delinsCTGCCAGTATCTG , LRG_274t1:c.2028_2040delinsCTGCCAGTATCTG NP_000518.1:p.Gly676=
NM_001195798.1:c.2028_2040delinsCTGCCAGTATCTG NP_001182727.1:p.Gly676=
NM_001195799.1:c.1905_1917delinsCTGCCAGTATCTG NP_001182728.1:p.Gly635=
NM_001195800.1:c.1524_1536delinsCTGCCAGTATCTG NP_001182729.1:p.Gly508=
NM_001195803.1:c.1606+177_1606+189delinsCTGCCAGTATCTG NP_001182732.1:n.1606+177_1606+189delinsCTGCCAGTATCTG
XM_011528010.1:c.2028_2040delinsCTGCCAGTATCTG XP_011526312.1:p.Gly676=
XM_011528011.1:c.1647_1659delinsCTGCCAGTATCTG XP_011526313.1:p.Gly549=
XR_244074.2:n.2038_2050delinsCTGCCAGTATCTG
XM_011528010.2:c.2028_2040delinsCTGCCAGTATCTG XP_011526312.1:p.Gly676=
XR_001753685.2:n.2145_2157delinsCTGCCAGTATCTG
XR_001753686.2:n.2005_2017delinsCTGCCAGTATCTG
NM_000527.5:c.2028_2040delinsCTGCCAGTATCTG MANE Select NP_000518.1:p.Gly676=
NM_001195798.2:c.2028_2040delinsCTGCCAGTATCTG NP_001182727.1:p.Gly676=
NM_001195799.2:c.1905_1917delinsCTGCCAGTATCTG NP_001182728.1:p.Gly635=
NM_001195800.2:c.1524_1536delinsCTGCCAGTATCTG NP_001182729.1:p.Gly508=
NM_001195803.2:c.1606+177_1606+189delinsCTGCCAGTATCTG NP_001182732.1:n.1606+177_1606+189delinsCTGCCAGTATCTG