Canonical Allele Identifier: CA2322780435
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129868_11129872delinsTAGAG , CM000681.2:g.11129868_11129872delinsTAGAG GRCh38
NC_000019.9:g.11240544_11240548delinsTAGAG , CM000681.1:g.11240544_11240548delinsTAGAG GRCh37
NC_000019.8:g.11101544_11101548delinsTAGAG NCBI36
NG_009060.1:g.45488_45492delinsTAGAG , LRG_274:g.45488_45492delinsTAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2805+198_2805+202delinsTAGAG ENSP00000252444.6:n.2805+198_2805+202delinsTAGAG
ENST00000559340.2:c.*616+198_*616+202delinsTAGAG ENSP00000453696.2:n.*616+198_*616+202delinsTAGAG
ENST00000560467.2:c.2427+198_2427+202delinsTAGAG ENSP00000453513.2:n.2427+198_2427+202delinsTAGAG
ENST00000558518.6:c.2547+198_2547+202delinsTAGAG MANE Select ENSP00000454071.1:n.2547+198_2547+202delinsTAGAG
ENST00000252444.9:c.2801+198_2801+202delinsTAGAG
ENST00000455727.6:c.2043+198_2043+202delinsTAGAG ENSP00000397829.2:n.2043+198_2043+202delinsTAGAG
ENST00000535915.5:c.2424+198_2424+202delinsTAGAG ENSP00000440520.1:n.2424+198_2424+202delinsTAGAG
ENST00000545707.5:c.2013+198_2013+202delinsTAGAG ENSP00000437639.1:n.2013+198_2013+202delinsTAGAG
ENST00000557933.5:c.2609+198_2609+202delinsTAGAG ENSP00000453557.1:n.2609+198_2609+202delinsTAGAG
ENST00000558013.5:c.2547+198_2547+202delinsTAGAG ENSP00000453346.1:n.2547+198_2547+202delinsTAGAG
ENST00000558518.5:c.2547+198_2547+202delinsTAGAG ENSP00000454071.1:n.2547+198_2547+202delinsTAGAG
ENST00000560628.1:n.108+2214_108+2218delinsTAGAG
NM_000527.4:c.2547+198_2547+202delinsTAGAG , LRG_274t1:c.2547+198_2547+202delinsTAGAG NP_000518.1:n.2547+198_2547+202delinsTAGAG
NM_001195798.1:c.2547+198_2547+202delinsTAGAG NP_001182727.1:n.2547+198_2547+202delinsTAGAG
NM_001195799.1:c.2424+198_2424+202delinsTAGAG NP_001182728.1:n.2424+198_2424+202delinsTAGAG
NM_001195800.1:c.2043+198_2043+202delinsTAGAG NP_001182729.1:n.2043+198_2043+202delinsTAGAG
NM_001195803.1:c.2013+198_2013+202delinsTAGAG NP_001182732.1:n.2013+198_2013+202delinsTAGAG
XM_011528010.1:c.2469+198_2469+202delinsTAGAG XP_011526312.1:n.2469+198_2469+202delinsTAGAG
XM_011528011.1:c.2166+198_2166+202delinsTAGAG XP_011526313.1:n.2166+198_2166+202delinsTAGAG
XM_011528010.2:c.2469+198_2469+202delinsTAGAG XP_011526312.1:n.2469+198_2469+202delinsTAGAG
XR_001753685.2:n.2881+198_2881+202delinsTAGAG
XR_001753686.2:n.2524+198_2524+202delinsTAGAG
NM_000527.5:c.2547+198_2547+202delinsTAGAG MANE Select NP_000518.1:n.2547+198_2547+202delinsTAGAG
NM_001195798.2:c.2547+198_2547+202delinsTAGAG NP_001182727.1:n.2547+198_2547+202delinsTAGAG
NM_001195799.2:c.2424+198_2424+202delinsTAGAG NP_001182728.1:n.2424+198_2424+202delinsTAGAG
NM_001195800.2:c.2043+198_2043+202delinsTAGAG NP_001182729.1:n.2043+198_2043+202delinsTAGAG
NM_001195803.2:c.2013+198_2013+202delinsTAGAG NP_001182732.1:n.2013+198_2013+202delinsTAGAG