Canonical Allele Identifier: CA404098419
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11240209C>G (hg19) chr19:g.11129533C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129533C>G , CM000681.2:g.11129533C>G GRCh38
NC_000019.9:g.11240209C>G , CM000681.1:g.11240209C>G GRCh37
NC_000019.8:g.11101209C>G NCBI36
NG_009060.1:g.45153C>G , LRG_274:g.45153C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2668C>G ENSP00000252444.6:p.Leu890Val
ENST00000559340.2:c.*479C>G ENSP00000453696.2:n.*479C>G
ENST00000560467.2:c.2290C>G ENSP00000453513.2:p.Leu764Val
ENST00000558518.6:c.2410C>G MANE Select ENSP00000454071.1:p.Leu804Val
ENST00000252444.9:c.2664C>G
ENST00000455727.6:c.1906C>G ENSP00000397829.2:p.Leu636Val
ENST00000535915.5:c.2287C>G ENSP00000440520.1:p.Leu763Val
ENST00000545707.5:c.1876C>G ENSP00000437639.1:p.Leu626Val
ENST00000557933.5:c.2472C>G ENSP00000453557.1:p.Ala824=
ENST00000558013.5:c.2410C>G ENSP00000453346.1:p.Leu804Val
ENST00000558518.5:c.2410C>G ENSP00000454071.1:p.Leu804Val
ENST00000560628.1:n.108+1879C>G
NM_000527.4:c.2410C>G , LRG_274t1:c.2410C>G NP_000518.1:p.Leu804Val
NM_001195798.1:c.2410C>G NP_001182727.1:p.Leu804Val
NM_001195799.1:c.2287C>G NP_001182728.1:p.Leu763Val
NM_001195800.1:c.1906C>G NP_001182729.1:p.Leu636Val
NM_001195803.1:c.1876C>G NP_001182732.1:p.Leu626Val
XM_011528010.1:c.2332C>G XP_011526312.1:p.Leu778Val
XM_011528011.1:c.2029C>G XP_011526313.1:p.Leu677Val
XR_244074.2:n.2420C>G
XM_011528010.2:c.2332C>G XP_011526312.1:p.Leu778Val
XR_001753685.2:n.2744C>G
XR_001753686.2:n.2387C>G
NM_000527.5:c.2410C>G MANE Select NP_000518.1:p.Leu804Val
NM_001195798.2:c.2410C>G NP_001182727.1:p.Leu804Val
NM_001195799.2:c.2287C>G NP_001182728.1:p.Leu763Val
NM_001195800.2:c.1906C>G NP_001182729.1:p.Leu636Val
NM_001195803.2:c.1876C>G NP_001182732.1:p.Leu626Val
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