Canonical Allele Identifier: CA404085779
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11224252C>G (hg19) chr19:g.11113576C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113576C>G , CM000681.2:g.11113576C>G GRCh38
NC_000019.9:g.11224252C>G , CM000681.1:g.11224252C>G GRCh37
NC_000019.8:g.11085252C>G NCBI36
NG_009060.1:g.29196C>G , LRG_274:g.29196C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1658C>G ENSP00000252444.6:p.Thr553Ser
ENST00000559340.2:c.1400C>G ENSP00000453696.2:p.Thr467Ser
ENST00000560467.2:c.1280C>G ENSP00000453513.2:p.Thr427Ser
ENST00000558518.6:c.1400C>G MANE Select ENSP00000454071.1:p.Thr467Ser
ENST00000252444.9:c.1654C>G
ENST00000455727.6:c.896C>G ENSP00000397829.2:p.Thr299Ser
ENST00000535915.5:c.1277C>G ENSP00000440520.1:p.Thr426Ser
ENST00000545707.5:c.1019C>G ENSP00000437639.1:p.Thr340Ser
ENST00000557933.5:c.1400C>G ENSP00000453557.1:p.Thr467Ser
ENST00000558013.5:c.1400C>G ENSP00000453346.1:p.Thr467Ser
ENST00000558518.5:c.1400C>G ENSP00000454071.1:p.Thr467Ser
ENST00000559340.1:c.121C>G
ENST00000560467.1:c.880C>G
NM_000527.4:c.1400C>G , LRG_274t1:c.1400C>G NP_000518.1:p.Thr467Ser
NM_001195798.1:c.1400C>G NP_001182727.1:p.Thr467Ser
NM_001195799.1:c.1277C>G NP_001182728.1:p.Thr426Ser
NM_001195800.1:c.896C>G NP_001182729.1:p.Thr299Ser
NM_001195803.1:c.1019C>G NP_001182732.1:p.Thr340Ser
XM_011528010.1:c.1400C>G XP_011526312.1:p.Thr467Ser
XM_011528011.1:c.1019C>G XP_011526313.1:p.Thr340Ser
XR_244074.2:n.1550C>G
XM_011528010.2:c.1400C>G XP_011526312.1:p.Thr467Ser
XR_001753685.2:n.1517C>G
XR_001753686.2:n.1517C>G
NM_000527.5:c.1400C>G MANE Select NP_000518.1:p.Thr467Ser
NM_001195798.2:c.1400C>G NP_001182727.1:p.Thr467Ser
NM_001195799.2:c.1277C>G NP_001182728.1:p.Thr426Ser
NM_001195800.2:c.896C>G NP_001182729.1:p.Thr299Ser
NM_001195803.2:c.1019C>G NP_001182732.1:p.Thr340Ser
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