Canonical Allele Identifier: CA404099241
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 1791856
ClinVar RCV Id: RCV002455579
MyVariant Identifiers: chr19:g.11240277C>G (hg19) chr19:g.11129601C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129601C>G , CM000681.2:g.11129601C>G GRCh38
NC_000019.9:g.11240277C>G , CM000681.1:g.11240277C>G GRCh37
NC_000019.8:g.11101277C>G NCBI36
NG_009060.1:g.45221C>G , LRG_274:g.45221C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2736C>G ENSP00000252444.6:p.Pro912=
ENST00000559340.2:c.*547C>G ENSP00000453696.2:n.*547C>G
ENST00000560467.2:c.2358C>G ENSP00000453513.2:p.Pro786=
ENST00000558518.6:c.2478C>G MANE Select ENSP00000454071.1:p.Pro826=
ENST00000252444.9:c.2732C>G
ENST00000455727.6:c.1974C>G ENSP00000397829.2:p.Pro658=
ENST00000535915.5:c.2355C>G ENSP00000440520.1:p.Pro785=
ENST00000545707.5:c.1944C>G ENSP00000437639.1:p.Pro648=
ENST00000557933.5:c.2540C>G ENSP00000453557.1:p.Pro847Arg
ENST00000558013.5:c.2478C>G ENSP00000453346.1:p.Pro826=
ENST00000558518.5:c.2478C>G ENSP00000454071.1:p.Pro826=
ENST00000560628.1:n.108+1947C>G
NM_000527.4:c.2478C>G , LRG_274t1:c.2478C>G NP_000518.1:p.Pro826=
NM_001195798.1:c.2478C>G NP_001182727.1:p.Pro826=
NM_001195799.1:c.2355C>G NP_001182728.1:p.Pro785=
NM_001195800.1:c.1974C>G NP_001182729.1:p.Pro658=
NM_001195803.1:c.1944C>G NP_001182732.1:p.Pro648=
XM_011528010.1:c.2400C>G XP_011526312.1:p.Pro800=
XM_011528011.1:c.2097C>G XP_011526313.1:p.Pro699=
XM_011528010.2:c.2400C>G XP_011526312.1:p.Pro800=
XR_001753685.2:n.2812C>G
XR_001753686.2:n.2455C>G
NM_000527.5:c.2478C>G MANE Select NP_000518.1:p.Pro826=
NM_001195798.2:c.2478C>G NP_001182727.1:p.Pro826=
NM_001195799.2:c.2355C>G NP_001182728.1:p.Pro785=
NM_001195800.2:c.1974C>G NP_001182729.1:p.Pro658=
NM_001195803.2:c.1944C>G NP_001182732.1:p.Pro648=
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