Canonical Allele Identifier: CA404099671
Gene: LDLR HGNC NCBI

Linked Data

gnomAD v4: 19-11129640-C-G
MyVariant Identifiers: chr19:g.11240316C>G (hg19) chr19:g.11129640C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129640C>G , CM000681.2:g.11129640C>G GRCh38
NC_000019.9:g.11240316C>G , CM000681.1:g.11240316C>G GRCh37
NC_000019.8:g.11101316C>G NCBI36
NG_009060.1:g.45260C>G , LRG_274:g.45260C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2775C>G ENSP00000252444.6:p.Cys925Trp
ENST00000559340.2:c.*586C>G ENSP00000453696.2:n.*586C>G
ENST00000560467.2:c.2397C>G ENSP00000453513.2:p.Cys799Trp
ENST00000558518.6:c.2517C>G MANE Select ENSP00000454071.1:p.Cys839Trp
ENST00000252444.9:c.2771C>G
ENST00000455727.6:c.2013C>G ENSP00000397829.2:p.Cys671Trp
ENST00000535915.5:c.2394C>G ENSP00000440520.1:p.Cys798Trp
ENST00000545707.5:c.1983C>G ENSP00000437639.1:p.Cys661Trp
ENST00000557933.5:c.2579C>G ENSP00000453557.1:p.Ala860Gly
ENST00000558013.5:c.2517C>G ENSP00000453346.1:p.Cys839Trp
ENST00000558518.5:c.2517C>G ENSP00000454071.1:p.Cys839Trp
ENST00000560628.1:n.108+1986C>G
NM_000527.4:c.2517C>G , LRG_274t1:c.2517C>G NP_000518.1:p.Cys839Trp
NM_001195798.1:c.2517C>G NP_001182727.1:p.Cys839Trp
NM_001195799.1:c.2394C>G NP_001182728.1:p.Cys798Trp
NM_001195800.1:c.2013C>G NP_001182729.1:p.Cys671Trp
NM_001195803.1:c.1983C>G NP_001182732.1:p.Cys661Trp
XM_011528010.1:c.2439C>G XP_011526312.1:p.Cys813Trp
XM_011528011.1:c.2136C>G XP_011526313.1:p.Cys712Trp
XM_011528010.2:c.2439C>G XP_011526312.1:p.Cys813Trp
XR_001753685.2:n.2851C>G
XR_001753686.2:n.2494C>G
NM_000527.5:c.2517C>G MANE Select NP_000518.1:p.Cys839Trp
NM_001195798.2:c.2517C>G NP_001182727.1:p.Cys839Trp
NM_001195799.2:c.2394C>G NP_001182728.1:p.Cys798Trp
NM_001195800.2:c.2013C>G NP_001182729.1:p.Cys671Trp
NM_001195803.2:c.1983C>G NP_001182732.1:p.Cys661Trp
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