Canonical Allele Identifier: CA2322777542
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs2077596309

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123860_11123861insCGAG , CM000681.2:g.11123860_11123861insCGAG GRCh38
NC_000019.9:g.11234536_11234537insCGAG , CM000681.1:g.11234536_11234537insCGAG GRCh37
NC_000019.8:g.11095536_11095537insCGAG NCBI36
NG_009060.1:g.39480_39481insCGAG , LRG_274:g.39480_39481insCGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2569+516_2569+517insCGAG ENSP00000252444.6:n.2569+516_2569+517insCGAG
ENST00000559340.2:c.*380+516_*380+517insCGAG ENSP00000453696.2:n.*380+516_*380+517insCGAG
ENST00000560467.2:c.2191+516_2191+517insCGAG ENSP00000453513.2:n.2191+516_2191+517insCGAG
ENST00000558518.6:c.2311+516_2311+517insCGAG MANE Select ENSP00000454071.1:n.2311+516_2311+517insCGAG
ENST00000252444.9:c.2565+516_2565+517insCGAG
ENST00000455727.6:c.1807+516_1807+517insCGAG ENSP00000397829.2:n.1807+516_1807+517insCGAG
ENST00000535915.5:c.2188+516_2188+517insCGAG ENSP00000440520.1:n.2188+516_2188+517insCGAG
ENST00000545707.5:c.1777+516_1777+517insCGAG ENSP00000437639.1:n.1777+516_1777+517insCGAG
ENST00000557933.5:c.2311+516_2311+517insCGAG ENSP00000453557.1:n.2311+516_2311+517insCGAG
ENST00000558013.5:c.2311+516_2311+517insCGAG ENSP00000453346.1:n.2311+516_2311+517insCGAG
ENST00000558518.5:c.2311+516_2311+517insCGAG ENSP00000454071.1:n.2311+516_2311+517insCGAG
NM_000527.4:c.2311+516_2311+517insCGAG , LRG_274t1:c.2311+516_2311+517insCGAG NP_000518.1:n.2311+516_2311+517insCGAG
NM_001195798.1:c.2311+516_2311+517insCGAG NP_001182727.1:n.2311+516_2311+517insCGAG
NM_001195799.1:c.2188+516_2188+517insCGAG NP_001182728.1:n.2188+516_2188+517insCGAG
NM_001195800.1:c.1807+516_1807+517insCGAG NP_001182729.1:n.1807+516_1807+517insCGAG
NM_001195803.1:c.1777+516_1777+517insCGAG NP_001182732.1:n.1777+516_1777+517insCGAG
XM_011528010.1:c.2311+516_2311+517insCGAG XP_011526312.1:n.2311+516_2311+517insCGAG
XM_011528011.1:c.1930+516_1930+517insCGAG XP_011526313.1:n.1930+516_1930+517insCGAG
XR_244074.2:n.2321+516_2321+517insCGAG
XM_011528010.2:c.2311+516_2311+517insCGAG XP_011526312.1:n.2311+516_2311+517insCGAG
XR_001753685.2:n.2645+516_2645+517insCGAG
XR_001753686.2:n.2288+516_2288+517insCGAG
NM_000527.5:c.2311+516_2311+517insCGAG MANE Select NP_000518.1:n.2311+516_2311+517insCGAG
NM_001195798.2:c.2311+516_2311+517insCGAG NP_001182727.1:n.2311+516_2311+517insCGAG
NM_001195799.2:c.2188+516_2188+517insCGAG NP_001182728.1:n.2188+516_2188+517insCGAG
NM_001195800.2:c.1807+516_1807+517insCGAG NP_001182729.1:n.1807+516_1807+517insCGAG
NM_001195803.2:c.1777+516_1777+517insCGAG NP_001182732.1:n.1777+516_1777+517insCGAG