Canonical Allele Identifier: CA404095768
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11234006C>G (hg19) chr19:g.11123330C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123330C>G , CM000681.2:g.11123330C>G GRCh38
NC_000019.9:g.11234006C>G , CM000681.1:g.11234006C>G GRCh37
NC_000019.8:g.11095006C>G NCBI36
NG_009060.1:g.38950C>G , LRG_274:g.38950C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2555C>G ENSP00000252444.6:p.Thr852Arg
ENST00000559340.2:c.*366C>G ENSP00000453696.2:n.*366C>G
ENST00000560467.2:c.2177C>G ENSP00000453513.2:p.Thr726Arg
ENST00000558518.6:c.2297C>G MANE Select ENSP00000454071.1:p.Thr766Arg
ENST00000252444.9:c.2551C>G
ENST00000455727.6:c.1793C>G ENSP00000397829.2:p.Thr598Arg
ENST00000535915.5:c.2174C>G ENSP00000440520.1:p.Thr725Arg
ENST00000545707.5:c.1763C>G ENSP00000437639.1:p.Thr588Arg
ENST00000557933.5:c.2297C>G ENSP00000453557.1:p.Thr766Arg
ENST00000558013.5:c.2297C>G ENSP00000453346.1:p.Thr766Arg
ENST00000558518.5:c.2297C>G ENSP00000454071.1:p.Thr766Arg
NM_000527.4:c.2297C>G , LRG_274t1:c.2297C>G NP_000518.1:p.Thr766Arg
NM_001195798.1:c.2297C>G NP_001182727.1:p.Thr766Arg
NM_001195799.1:c.2174C>G NP_001182728.1:p.Thr725Arg
NM_001195800.1:c.1793C>G NP_001182729.1:p.Thr598Arg
NM_001195803.1:c.1763C>G NP_001182732.1:p.Thr588Arg
XM_011528010.1:c.2297C>G XP_011526312.1:p.Thr766Arg
XM_011528011.1:c.1916C>G XP_011526313.1:p.Thr639Arg
XR_244074.2:n.2307C>G
XM_011528010.2:c.2297C>G XP_011526312.1:p.Thr766Arg
XR_001753685.2:n.2631C>G
XR_001753686.2:n.2274C>G
NM_000527.5:c.2297C>G MANE Select NP_000518.1:p.Thr766Arg
NM_001195798.2:c.2297C>G NP_001182727.1:p.Thr766Arg
NM_001195799.2:c.2174C>G NP_001182728.1:p.Thr725Arg
NM_001195800.2:c.1793C>G NP_001182729.1:p.Thr598Arg
NM_001195803.2:c.1763C>G NP_001182732.1:p.Thr588Arg
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