Canonical Allele Identifier: CA505484963
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11217350T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11106674T>G , CM000681.2:g.11106674T>G GRCh38
NC_000019.9:g.11217350T>G , CM000681.1:g.11217350T>G GRCh37
NC_000019.8:g.11078350T>G NCBI36
NG_009060.1:g.22294T>G , LRG_274:g.22294T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1062T>G ENSP00000252444.6:p.Val354=
ENST00000559340.2:c.804T>G ENSP00000453696.2:p.Val268=
ENST00000560467.2:c.804T>G ENSP00000453513.2:p.Val268=
ENST00000558518.6:c.804T>G MANE Select ENSP00000454071.1:p.Val268=
ENST00000252444.9:c.1058T>G
ENST00000455727.6:c.314-718T>G ENSP00000397829.2:n.314-718T>G
ENST00000535915.5:c.681T>G ENSP00000440520.1:p.Val227=
ENST00000545707.5:c.423T>G ENSP00000437639.1:p.Val141=
ENST00000557933.5:c.804T>G ENSP00000453557.1:p.Val268=
ENST00000558013.5:c.804T>G ENSP00000453346.1:p.Val268=
ENST00000558518.5:c.804T>G ENSP00000454071.1:p.Val268=
ENST00000558528.1:n.319T>G
ENST00000560467.1:c.404T>G
NM_000527.4:c.804T>G , LRG_274t1:c.804T>G NP_000518.1:p.Val268=
NM_001195798.1:c.804T>G NP_001182727.1:p.Val268=
NM_001195799.1:c.681T>G NP_001182728.1:p.Val227=
NM_001195800.1:c.314-718T>G NP_001182729.1:n.314-718T>G
NM_001195803.1:c.423T>G NP_001182732.1:p.Val141=
XM_011528010.1:c.804T>G XP_011526312.1:p.Val268=
XM_011528011.1:c.423T>G XP_011526313.1:p.Val141=
XR_244074.2:n.954T>G
XM_011528010.2:c.804T>G XP_011526312.1:p.Val268=
XR_001753685.2:n.921T>G
XR_001753686.2:n.921T>G
NM_000527.5:c.804T>G MANE Select NP_000518.1:p.Val268=
NM_001195798.2:c.804T>G NP_001182727.1:p.Val268=
NM_001195799.2:c.681T>G NP_001182728.1:p.Val227=
NM_001195800.2:c.314-718T>G NP_001182729.1:n.314-718T>G
NM_001195803.2:c.423T>G NP_001182732.1:p.Val141=
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