Canonical Allele Identifier: CA2322780423
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129846A= , CM000681.2:g.11129846A= GRCh38
NC_000019.9:g.11240522A= , CM000681.1:g.11240522A= GRCh37
NC_000019.8:g.11101522A= NCBI36
NG_009060.1:g.45466A= , LRG_274:g.45466A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2805+176A= ENSP00000252444.6:n.2805+176A=
ENST00000559340.2:c.*616+176A= ENSP00000453696.2:n.*616+176A=
ENST00000560467.2:c.2427+176A= ENSP00000453513.2:n.2427+176A=
ENST00000558518.6:c.2547+176A= MANE Select ENSP00000454071.1:n.2547+176A=
ENST00000252444.9:c.2801+176A=
ENST00000455727.6:c.2043+176A= ENSP00000397829.2:n.2043+176A=
ENST00000535915.5:c.2424+176A= ENSP00000440520.1:n.2424+176A=
ENST00000545707.5:c.2013+176A= ENSP00000437639.1:n.2013+176A=
ENST00000557933.5:c.2609+176A= ENSP00000453557.1:n.2609+176A=
ENST00000558013.5:c.2547+176A= ENSP00000453346.1:n.2547+176A=
ENST00000558518.5:c.2547+176A= ENSP00000454071.1:n.2547+176A=
ENST00000560628.1:n.108+2192A=
NM_000527.4:c.2547+176A= , LRG_274t1:c.2547+176A= NP_000518.1:n.2547+176A=
NM_001195798.1:c.2547+176A= NP_001182727.1:n.2547+176A=
NM_001195799.1:c.2424+176A= NP_001182728.1:n.2424+176A=
NM_001195800.1:c.2043+176A= NP_001182729.1:n.2043+176A=
NM_001195803.1:c.2013+176A= NP_001182732.1:n.2013+176A=
XM_011528010.1:c.2469+176A= XP_011526312.1:n.2469+176A=
XM_011528011.1:c.2166+176A= XP_011526313.1:n.2166+176A=
XM_011528010.2:c.2469+176A= XP_011526312.1:n.2469+176A=
XR_001753685.2:n.2881+176A=
XR_001753686.2:n.2524+176A=
NM_000527.5:c.2547+176A= MANE Select NP_000518.1:n.2547+176A=
NM_001195798.2:c.2547+176A= NP_001182727.1:n.2547+176A=
NM_001195799.2:c.2424+176A= NP_001182728.1:n.2424+176A=
NM_001195800.2:c.2043+176A= NP_001182729.1:n.2043+176A=
NM_001195803.2:c.2013+176A= NP_001182732.1:n.2013+176A=