Canonical Allele Identifier: CA404098665
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11240227T>G (hg19) chr19:g.11129551T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129551T>G , CM000681.2:g.11129551T>G GRCh38
NC_000019.9:g.11240227T>G , CM000681.1:g.11240227T>G GRCh37
NC_000019.8:g.11101227T>G NCBI36
NG_009060.1:g.45171T>G , LRG_274:g.45171T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2686T>G ENSP00000252444.6:p.Trp896Gly
ENST00000559340.2:c.*497T>G ENSP00000453696.2:n.*497T>G
ENST00000560467.2:c.2308T>G ENSP00000453513.2:p.Trp770Gly
ENST00000558518.6:c.2428T>G MANE Select ENSP00000454071.1:p.Trp810Gly
ENST00000252444.9:c.2682T>G
ENST00000455727.6:c.1924T>G ENSP00000397829.2:p.Trp642Gly
ENST00000535915.5:c.2305T>G ENSP00000440520.1:p.Trp769Gly
ENST00000545707.5:c.1894T>G ENSP00000437639.1:p.Trp632Gly
ENST00000557933.5:c.2490T>G ENSP00000453557.1:p.Tyr830Ter
ENST00000558013.5:c.2428T>G ENSP00000453346.1:p.Trp810Gly
ENST00000558518.5:c.2428T>G ENSP00000454071.1:p.Trp810Gly
ENST00000560628.1:n.108+1897T>G
NM_000527.4:c.2428T>G , LRG_274t1:c.2428T>G NP_000518.1:p.Trp810Gly
NM_001195798.1:c.2428T>G NP_001182727.1:p.Trp810Gly
NM_001195799.1:c.2305T>G NP_001182728.1:p.Trp769Gly
NM_001195800.1:c.1924T>G NP_001182729.1:p.Trp642Gly
NM_001195803.1:c.1894T>G NP_001182732.1:p.Trp632Gly
XM_011528010.1:c.2350T>G XP_011526312.1:p.Trp784Gly
XM_011528011.1:c.2047T>G XP_011526313.1:p.Trp683Gly
XR_244074.2:n.2438T>G
XM_011528010.2:c.2350T>G XP_011526312.1:p.Trp784Gly
XR_001753685.2:n.2762T>G
XR_001753686.2:n.2405T>G
NM_000527.5:c.2428T>G MANE Select NP_000518.1:p.Trp810Gly
NM_001195798.2:c.2428T>G NP_001182727.1:p.Trp810Gly
NM_001195799.2:c.2305T>G NP_001182728.1:p.Trp769Gly
NM_001195800.2:c.1924T>G NP_001182729.1:p.Trp642Gly
NM_001195803.2:c.1894T>G NP_001182732.1:p.Trp632Gly
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