Canonical Allele Identifier: CA404099123
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11240266T>G (hg19) chr19:g.11129590T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129590T>G , CM000681.2:g.11129590T>G GRCh38
NC_000019.9:g.11240266T>G , CM000681.1:g.11240266T>G GRCh37
NC_000019.8:g.11101266T>G NCBI36
NG_009060.1:g.45210T>G , LRG_274:g.45210T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2725T>G ENSP00000252444.6:p.Phe909Val
ENST00000559340.2:c.*536T>G ENSP00000453696.2:n.*536T>G
ENST00000560467.2:c.2347T>G ENSP00000453513.2:p.Phe783Val
ENST00000558518.6:c.2467T>G MANE Select ENSP00000454071.1:p.Phe823Val
ENST00000252444.9:c.2721T>G
ENST00000455727.6:c.1963T>G ENSP00000397829.2:p.Phe655Val
ENST00000535915.5:c.2344T>G ENSP00000440520.1:p.Phe782Val
ENST00000545707.5:c.1933T>G ENSP00000437639.1:p.Phe645Val
ENST00000557933.5:c.2529T>G ENSP00000453557.1:p.Thr843=
ENST00000558013.5:c.2467T>G ENSP00000453346.1:p.Phe823Val
ENST00000558518.5:c.2467T>G ENSP00000454071.1:p.Phe823Val
ENST00000560628.1:n.108+1936T>G
NM_000527.4:c.2467T>G , LRG_274t1:c.2467T>G NP_000518.1:p.Phe823Val
NM_001195798.1:c.2467T>G NP_001182727.1:p.Phe823Val
NM_001195799.1:c.2344T>G NP_001182728.1:p.Phe782Val
NM_001195800.1:c.1963T>G NP_001182729.1:p.Phe655Val
NM_001195803.1:c.1933T>G NP_001182732.1:p.Phe645Val
XM_011528010.1:c.2389T>G XP_011526312.1:p.Phe797Val
XM_011528011.1:c.2086T>G XP_011526313.1:p.Phe696Val
XM_011528010.2:c.2389T>G XP_011526312.1:p.Phe797Val
XR_001753685.2:n.2801T>G
XR_001753686.2:n.2444T>G
NM_000527.5:c.2467T>G MANE Select NP_000518.1:p.Phe823Val
NM_001195798.2:c.2467T>G NP_001182727.1:p.Phe823Val
NM_001195799.2:c.2344T>G NP_001182728.1:p.Phe782Val
NM_001195800.2:c.1963T>G NP_001182729.1:p.Phe655Val
NM_001195803.2:c.1933T>G NP_001182732.1:p.Phe645Val
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