Canonical Allele Identifier: CA2322779353
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11127718_11127736delinsCTGAGGCAGGAGGATCTCT , CM000681.2:g.11127718_11127736delinsCTGAGGCAGGAGGATCTCT GRCh38
NC_000019.9:g.11238394_11238412delinsCTGAGGCAGGAGGATCTCT , CM000681.1:g.11238394_11238412delinsCTGAGGCAGGAGGATCTCT GRCh37
NC_000019.8:g.11099394_11099412delinsCTGAGGCAGGAGGATCTCT NCBI36
NG_009060.1:g.43338_43356delinsCTGAGGCAGGAGGATCTCT , LRG_274:g.43338_43356delinsCTGAGGCAGGAGGATCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2570-290_2570-272delinsCTGAGGCAGGAGGATCTCT ENSP00000252444.6:n.2570-290_2570-272delinsCTGAGGCAGGAGGATCTC...
ENST00000559340.2:c.*381-290_*381-272delinsCTGAGGCAGGAGGATCTCT ENSP00000453696.2:n.*381-290_*381-272delinsCTGAGGCAGGAGGATCTC...
ENST00000560467.2:c.2192-290_2192-272delinsCTGAGGCAGGAGGATCTCT ENSP00000453513.2:n.2192-290_2192-272delinsCTGAGGCAGGAGGATCTC...
ENST00000558518.6:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT MANE Select ENSP00000454071.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTC...
ENST00000252444.9:c.2566-290_2566-272delinsCTGAGGCAGGAGGATCTCT
ENST00000455727.6:c.1808-290_1808-272delinsCTGAGGCAGGAGGATCTCT ENSP00000397829.2:n.1808-290_1808-272delinsCTGAGGCAGGAGGATCTC...
ENST00000535915.5:c.2189-290_2189-272delinsCTGAGGCAGGAGGATCTCT ENSP00000440520.1:n.2189-290_2189-272delinsCTGAGGCAGGAGGATCTC...
ENST00000545707.5:c.1778-290_1778-272delinsCTGAGGCAGGAGGATCTCT ENSP00000437639.1:n.1778-290_1778-272delinsCTGAGGCAGGAGGATCTC...
ENST00000557933.5:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT ENSP00000453557.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTC...
ENST00000558013.5:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT ENSP00000453346.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTC...
ENST00000558518.5:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT ENSP00000454071.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTC...
ENST00000560628.1:n.108+64_108+82delinsCTGAGGCAGGAGGATCTCT
NM_000527.4:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT , LRG_274t1:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT NP_000518.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT
NM_001195798.1:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT NP_001182727.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT
NM_001195799.1:c.2189-290_2189-272delinsCTGAGGCAGGAGGATCTCT NP_001182728.1:n.2189-290_2189-272delinsCTGAGGCAGGAGGATCTCT
NM_001195800.1:c.1808-290_1808-272delinsCTGAGGCAGGAGGATCTCT NP_001182729.1:n.1808-290_1808-272delinsCTGAGGCAGGAGGATCTCT
NM_001195803.1:c.1778-290_1778-272delinsCTGAGGCAGGAGGATCTCT NP_001182732.1:n.1778-290_1778-272delinsCTGAGGCAGGAGGATCTCT
XM_011528010.1:c.2312-1795_2312-1777delinsCTGAGGCAGGAGGATCTCT XP_011526312.1:n.2312-1795_2312-1777delinsCTGAGGCAGGAGGATCTCT...
XM_011528011.1:c.1931-290_1931-272delinsCTGAGGCAGGAGGATCTCT XP_011526313.1:n.1931-290_1931-272delinsCTGAGGCAGGAGGATCTCT
XR_244074.2:n.2322-290_2322-272delinsCTGAGGCAGGAGGATCTCT
XM_011528010.2:c.2312-1795_2312-1777delinsCTGAGGCAGGAGGATCTCT XP_011526312.1:n.2312-1795_2312-1777delinsCTGAGGCAGGAGGATCTCT...
XR_001753685.2:n.2646-290_2646-272delinsCTGAGGCAGGAGGATCTCT
XR_001753686.2:n.2289-290_2289-272delinsCTGAGGCAGGAGGATCTCT
NM_000527.5:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT MANE Select NP_000518.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT
NM_001195798.2:c.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT NP_001182727.1:n.2312-290_2312-272delinsCTGAGGCAGGAGGATCTCT
NM_001195799.2:c.2189-290_2189-272delinsCTGAGGCAGGAGGATCTCT NP_001182728.1:n.2189-290_2189-272delinsCTGAGGCAGGAGGATCTCT
NM_001195800.2:c.1808-290_1808-272delinsCTGAGGCAGGAGGATCTCT NP_001182729.1:n.1808-290_1808-272delinsCTGAGGCAGGAGGATCTCT
NM_001195803.2:c.1778-290_1778-272delinsCTGAGGCAGGAGGATCTCT NP_001182732.1:n.1778-290_1778-272delinsCTGAGGCAGGAGGATCTCT