Canonical Allele Identifier: CA2322770948
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11111939_11111940delinsGA , CM000681.2:g.11111939_11111940delinsGA GRCh38
NC_000019.9:g.11222615_11222616delinsGA , CM000681.1:g.11222615_11222616delinsGA GRCh37
NC_000019.8:g.11083615_11083616delinsGA NCBI36
NG_009060.1:g.27559_27560delinsGA , LRG_274:g.27559_27560delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1444+300_1444+301delinsGA ENSP00000252444.6:n.1444+300_1444+301delinsGA
ENST00000559340.2:c.1186+300_1186+301delinsGA ENSP00000453696.2:n.1186+300_1186+301delinsGA
ENST00000560467.2:c.1066+300_1066+301delinsGA ENSP00000453513.2:n.1066+300_1066+301delinsGA
ENST00000558518.6:c.1186+300_1186+301delinsGA MANE Select ENSP00000454071.1:n.1186+300_1186+301delinsGA
ENST00000252444.9:c.1440+300_1440+301delinsGA
ENST00000455727.6:c.682+300_682+301delinsGA ENSP00000397829.2:n.682+300_682+301delinsGA
ENST00000535915.5:c.1063+300_1063+301delinsGA ENSP00000440520.1:n.1063+300_1063+301delinsGA
ENST00000545707.5:c.805+300_805+301delinsGA ENSP00000437639.1:n.805+300_805+301delinsGA
ENST00000557933.5:c.1186+300_1186+301delinsGA ENSP00000453557.1:n.1186+300_1186+301delinsGA
ENST00000558013.5:c.1186+300_1186+301delinsGA ENSP00000453346.1:n.1186+300_1186+301delinsGA
ENST00000558518.5:c.1186+300_1186+301delinsGA ENSP00000454071.1:n.1186+300_1186+301delinsGA
ENST00000560173.1:n.185+300_185+301delinsGA
ENST00000560467.1:c.666+300_666+301delinsGA
NM_000527.4:c.1186+300_1186+301delinsGA , LRG_274t1:c.1186+300_1186+301delinsGA NP_000518.1:n.1186+300_1186+301delinsGA
NM_001195798.1:c.1186+300_1186+301delinsGA NP_001182727.1:n.1186+300_1186+301delinsGA
NM_001195799.1:c.1063+300_1063+301delinsGA NP_001182728.1:n.1063+300_1063+301delinsGA
NM_001195800.1:c.682+300_682+301delinsGA NP_001182729.1:n.682+300_682+301delinsGA
NM_001195803.1:c.805+300_805+301delinsGA NP_001182732.1:n.805+300_805+301delinsGA
XM_011528010.1:c.1186+300_1186+301delinsGA XP_011526312.1:n.1186+300_1186+301delinsGA
XM_011528011.1:c.805+300_805+301delinsGA XP_011526313.1:n.805+300_805+301delinsGA
XR_244074.2:n.1336+300_1336+301delinsGA
XM_011528010.2:c.1186+300_1186+301delinsGA XP_011526312.1:n.1186+300_1186+301delinsGA
XR_001753685.2:n.1303+300_1303+301delinsGA
XR_001753686.2:n.1303+300_1303+301delinsGA
NM_000527.5:c.1186+300_1186+301delinsGA MANE Select NP_000518.1:n.1186+300_1186+301delinsGA
NM_001195798.2:c.1186+300_1186+301delinsGA NP_001182727.1:n.1186+300_1186+301delinsGA
NM_001195799.2:c.1063+300_1063+301delinsGA NP_001182728.1:n.1063+300_1063+301delinsGA
NM_001195800.2:c.682+300_682+301delinsGA NP_001182729.1:n.682+300_682+301delinsGA
NM_001195803.2:c.805+300_805+301delinsGA NP_001182732.1:n.805+300_805+301delinsGA