Canonical Allele Identifier: CA631764682
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs1438834022

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11108229_11108230insG , CM000681.2:g.11108229_11108230insG GRCh38
NC_000019.9:g.11218905_11218906insG , CM000681.1:g.11218905_11218906insG GRCh37
NC_000019.8:g.11079905_11079906insG NCBI36
NG_009060.1:g.23849_23850insG , LRG_274:g.23849_23850insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1198+715_1198+716insG ENSP00000252444.6:n.1198+715_1198+716insG
ENST00000559340.2:c.940+715_940+716insG ENSP00000453696.2:n.940+715_940+716insG
ENST00000560467.2:c.940+715_940+716insG ENSP00000453513.2:n.940+715_940+716insG
ENST00000558518.6:c.940+715_940+716insG MANE Select ENSP00000454071.1:n.940+715_940+716insG
ENST00000252444.9:c.1194+715_1194+716insG
ENST00000455727.6:c.436+715_436+716insG ENSP00000397829.2:n.436+715_436+716insG
ENST00000535915.5:c.817+715_817+716insG ENSP00000440520.1:n.817+715_817+716insG
ENST00000545707.5:c.559+715_559+716insG ENSP00000437639.1:n.559+715_559+716insG
ENST00000557933.5:c.940+715_940+716insG ENSP00000453557.1:n.940+715_940+716insG
ENST00000558013.5:c.940+715_940+716insG ENSP00000453346.1:n.940+715_940+716insG
ENST00000558518.5:c.940+715_940+716insG ENSP00000454071.1:n.940+715_940+716insG
ENST00000560467.1:c.540+715_540+716insG
NM_000527.4:c.940+715_940+716insG , LRG_274t1:c.940+715_940+716insG NP_000518.1:n.940+715_940+716insG
NM_001195798.1:c.940+715_940+716insG NP_001182727.1:n.940+715_940+716insG
NM_001195799.1:c.817+715_817+716insG NP_001182728.1:n.817+715_817+716insG
NM_001195800.1:c.436+715_436+716insG NP_001182729.1:n.436+715_436+716insG
NM_001195803.1:c.559+715_559+716insG NP_001182732.1:n.559+715_559+716insG
XM_011528010.1:c.940+715_940+716insG XP_011526312.1:n.940+715_940+716insG
XM_011528011.1:c.559+715_559+716insG XP_011526313.1:n.559+715_559+716insG
XR_244074.2:n.1090+715_1090+716insG
XM_011528010.2:c.940+715_940+716insG XP_011526312.1:n.940+715_940+716insG
XR_001753685.2:n.1057+715_1057+716insG
XR_001753686.2:n.1057+715_1057+716insG
NM_000527.5:c.940+715_940+716insG MANE Select NP_000518.1:n.940+715_940+716insG
NM_001195798.2:c.940+715_940+716insG NP_001182727.1:n.940+715_940+716insG
NM_001195799.2:c.817+715_817+716insG NP_001182728.1:n.817+715_817+716insG
NM_001195800.2:c.436+715_436+716insG NP_001182729.1:n.436+715_436+716insG
NM_001195803.2:c.559+715_559+716insG NP_001182732.1:n.559+715_559+716insG