Canonical Allele Identifier: CA2813590520
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11108221_11108222insC , CM000681.2:g.11108221_11108222insC GRCh38
NC_000019.9:g.11218897_11218898insC , CM000681.1:g.11218897_11218898insC GRCh37
NC_000019.8:g.11079897_11079898insC NCBI36
NG_009060.1:g.23841_23842insC , LRG_274:g.23841_23842insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1198+707_1198+708insC ENSP00000252444.6:n.1198+707_1198+708insC
ENST00000559340.2:c.940+707_940+708insC ENSP00000453696.2:n.940+707_940+708insC
ENST00000560467.2:c.940+707_940+708insC ENSP00000453513.2:n.940+707_940+708insC
ENST00000558518.6:c.940+707_940+708insC MANE Select ENSP00000454071.1:n.940+707_940+708insC
ENST00000252444.9:c.1194+707_1194+708insC
ENST00000455727.6:c.436+707_436+708insC ENSP00000397829.2:n.436+707_436+708insC
ENST00000535915.5:c.817+707_817+708insC ENSP00000440520.1:n.817+707_817+708insC
ENST00000545707.5:c.559+707_559+708insC ENSP00000437639.1:n.559+707_559+708insC
ENST00000557933.5:c.940+707_940+708insC ENSP00000453557.1:n.940+707_940+708insC
ENST00000558013.5:c.940+707_940+708insC ENSP00000453346.1:n.940+707_940+708insC
ENST00000558518.5:c.940+707_940+708insC ENSP00000454071.1:n.940+707_940+708insC
ENST00000560467.1:c.540+707_540+708insC
NM_000527.4:c.940+707_940+708insC , LRG_274t1:c.940+707_940+708insC NP_000518.1:n.940+707_940+708insC
NM_001195798.1:c.940+707_940+708insC NP_001182727.1:n.940+707_940+708insC
NM_001195799.1:c.817+707_817+708insC NP_001182728.1:n.817+707_817+708insC
NM_001195800.1:c.436+707_436+708insC NP_001182729.1:n.436+707_436+708insC
NM_001195803.1:c.559+707_559+708insC NP_001182732.1:n.559+707_559+708insC
XM_011528010.1:c.940+707_940+708insC XP_011526312.1:n.940+707_940+708insC
XM_011528011.1:c.559+707_559+708insC XP_011526313.1:n.559+707_559+708insC
XR_244074.2:n.1090+707_1090+708insC
XM_011528010.2:c.940+707_940+708insC XP_011526312.1:n.940+707_940+708insC
XR_001753685.2:n.1057+707_1057+708insC
XR_001753686.2:n.1057+707_1057+708insC
NM_000527.5:c.940+707_940+708insC MANE Select NP_000518.1:n.940+707_940+708insC
NM_001195798.2:c.940+707_940+708insC NP_001182727.1:n.940+707_940+708insC
NM_001195799.2:c.817+707_817+708insC NP_001182728.1:n.817+707_817+708insC
NM_001195800.2:c.436+707_436+708insC NP_001182729.1:n.436+707_436+708insC
NM_001195803.2:c.559+707_559+708insC NP_001182732.1:n.559+707_559+708insC