Canonical Allele Identifier: CA993527494
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11100483_11100484insGTGAGCC , CM000681.2:g.11100483_11100484insGTGAGCC GRCh38
NC_000019.9:g.11211159_11211160insGTGAGCC , CM000681.1:g.11211159_11211160insGTGAGCC GRCh37
NC_000019.8:g.11072159_11072160insGTGAGCC NCBI36
NG_009060.1:g.16103_16104insGTGAGCC , LRG_274:g.16103_16104insGTGAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.448+138_448+139insGTGAGCC ENSP00000252444.6:n.448+138_448+139insGTGAGCC
ENST00000559340.2:c.190+138_190+139insGTGAGCC ENSP00000453696.2:n.190+138_190+139insGTGAGCC
ENST00000560467.2:c.190+138_190+139insGTGAGCC ENSP00000453513.2:n.190+138_190+139insGTGAGCC
ENST00000558518.6:c.190+138_190+139insGTGAGCC MANE Select ENSP00000454071.1:n.190+138_190+139insGTGAGCC
ENST00000252444.9:c.444+138_444+139insGTGAGCC
ENST00000455727.6:c.190+138_190+139insGTGAGCC ENSP00000397829.2:n.190+138_190+139insGTGAGCC
ENST00000535915.5:c.190+138_190+139insGTGAGCC ENSP00000440520.1:n.190+138_190+139insGTGAGCC
ENST00000545707.5:c.190+138_190+139insGTGAGCC ENSP00000437639.1:n.190+138_190+139insGTGAGCC
ENST00000557933.5:c.190+138_190+139insGTGAGCC ENSP00000453557.1:n.190+138_190+139insGTGAGCC
ENST00000557958.1:n.276+138_276+139insGTGAGCC
ENST00000558013.5:c.190+138_190+139insGTGAGCC ENSP00000453346.1:n.190+138_190+139insGTGAGCC
ENST00000558518.5:c.190+138_190+139insGTGAGCC ENSP00000454071.1:n.190+138_190+139insGTGAGCC
ENST00000560502.5:n.414_415insGTGAGCC
NM_000527.4:c.190+138_190+139insGTGAGCC , LRG_274t1:c.190+138_190+139insGTGAGCC NP_000518.1:n.190+138_190+139insGTGAGCC
NM_001195798.1:c.190+138_190+139insGTGAGCC NP_001182727.1:n.190+138_190+139insGTGAGCC
NM_001195799.1:c.190+138_190+139insGTGAGCC NP_001182728.1:n.190+138_190+139insGTGAGCC
NM_001195800.1:c.190+138_190+139insGTGAGCC NP_001182729.1:n.190+138_190+139insGTGAGCC
NM_001195803.1:c.190+138_190+139insGTGAGCC NP_001182732.1:n.190+138_190+139insGTGAGCC
XM_011528010.1:c.190+138_190+139insGTGAGCC XP_011526312.1:n.190+138_190+139insGTGAGCC
XM_011528011.1:c.190+138_190+139insGTGAGCC XP_011526313.1:n.190+138_190+139insGTGAGCC
XR_244074.2:n.340+138_340+139insGTGAGCC
XM_011528010.2:c.190+138_190+139insGTGAGCC XP_011526312.1:n.190+138_190+139insGTGAGCC
XR_001753685.2:n.307+138_307+139insGTGAGCC
XR_001753686.2:n.307+138_307+139insGTGAGCC
NM_000527.5:c.190+138_190+139insGTGAGCC MANE Select NP_000518.1:n.190+138_190+139insGTGAGCC
NM_001195798.2:c.190+138_190+139insGTGAGCC NP_001182727.1:n.190+138_190+139insGTGAGCC
NM_001195799.2:c.190+138_190+139insGTGAGCC NP_001182728.1:n.190+138_190+139insGTGAGCC
NM_001195800.2:c.190+138_190+139insGTGAGCC NP_001182729.1:n.190+138_190+139insGTGAGCC
NM_001195803.2:c.190+138_190+139insGTGAGCC NP_001182732.1:n.190+138_190+139insGTGAGCC