Canonical Allele Identifier: CA2322780116
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129259_11129263delinsAGACT , CM000681.2:g.11129259_11129263delinsAGACT GRCh38
NC_000019.9:g.11239935_11239939delinsAGACT , CM000681.1:g.11239935_11239939delinsAGACT GRCh37
NC_000019.8:g.11100935_11100939delinsAGACT NCBI36
NG_009060.1:g.44879_44883delinsAGACT , LRG_274:g.44879_44883delinsAGACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2648-254_2648-250delinsAGACT ENSP00000252444.6:n.2648-254_2648-250delinsAGACT
ENST00000559340.2:c.*459-254_*459-250delinsAGACT ENSP00000453696.2:n.*459-254_*459-250delinsAGACT
ENST00000560467.2:c.2270-254_2270-250delinsAGACT ENSP00000453513.2:n.2270-254_2270-250delinsAGACT
ENST00000558518.6:c.2390-254_2390-250delinsAGACT MANE Select ENSP00000454071.1:n.2390-254_2390-250delinsAGACT
ENST00000252444.9:c.2644-254_2644-250delinsAGACT
ENST00000455727.6:c.1886-254_1886-250delinsAGACT ENSP00000397829.2:n.1886-254_1886-250delinsAGACT
ENST00000535915.5:c.2267-254_2267-250delinsAGACT ENSP00000440520.1:n.2267-254_2267-250delinsAGACT
ENST00000545707.5:c.1856-254_1856-250delinsAGACT ENSP00000437639.1:n.1856-254_1856-250delinsAGACT
ENST00000557933.5:c.2390-192_2390-188delinsAGACT ENSP00000453557.1:n.2390-192_2390-188delinsAGACT
ENST00000558013.5:c.2390-254_2390-250delinsAGACT ENSP00000453346.1:n.2390-254_2390-250delinsAGACT
ENST00000558518.5:c.2390-254_2390-250delinsAGACT ENSP00000454071.1:n.2390-254_2390-250delinsAGACT
ENST00000560628.1:n.108+1605_108+1609delinsAGACT
NM_000527.4:c.2390-254_2390-250delinsAGACT , LRG_274t1:c.2390-254_2390-250delinsAGACT NP_000518.1:n.2390-254_2390-250delinsAGACT
NM_001195798.1:c.2390-254_2390-250delinsAGACT NP_001182727.1:n.2390-254_2390-250delinsAGACT
NM_001195799.1:c.2267-254_2267-250delinsAGACT NP_001182728.1:n.2267-254_2267-250delinsAGACT
NM_001195800.1:c.1886-254_1886-250delinsAGACT NP_001182729.1:n.1886-254_1886-250delinsAGACT
NM_001195803.1:c.1856-254_1856-250delinsAGACT NP_001182732.1:n.1856-254_1856-250delinsAGACT
XM_011528010.1:c.2312-254_2312-250delinsAGACT XP_011526312.1:n.2312-254_2312-250delinsAGACT
XM_011528011.1:c.2009-254_2009-250delinsAGACT XP_011526313.1:n.2009-254_2009-250delinsAGACT
XR_244074.2:n.2400-254_2400-250delinsAGACT
XM_011528010.2:c.2312-254_2312-250delinsAGACT XP_011526312.1:n.2312-254_2312-250delinsAGACT
XR_001753685.2:n.2724-254_2724-250delinsAGACT
XR_001753686.2:n.2367-254_2367-250delinsAGACT
NM_000527.5:c.2390-254_2390-250delinsAGACT MANE Select NP_000518.1:n.2390-254_2390-250delinsAGACT
NM_001195798.2:c.2390-254_2390-250delinsAGACT NP_001182727.1:n.2390-254_2390-250delinsAGACT
NM_001195799.2:c.2267-254_2267-250delinsAGACT NP_001182728.1:n.2267-254_2267-250delinsAGACT
NM_001195800.2:c.1886-254_1886-250delinsAGACT NP_001182729.1:n.1886-254_1886-250delinsAGACT
NM_001195803.2:c.1856-254_1856-250delinsAGACT NP_001182732.1:n.1856-254_1856-250delinsAGACT