Canonical Allele Identifier: CA505743462
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11231068C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120392C>G , CM000681.2:g.11120392C>G GRCh38
NC_000019.9:g.11231068C>G , CM000681.1:g.11231068C>G GRCh37
NC_000019.8:g.11092068C>G NCBI36
NG_009060.1:g.36012C>G , LRG_274:g.36012C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2268C>G ENSP00000252444.6:p.Thr756=
ENST00000559340.2:c.*79C>G ENSP00000453696.2:n.*79C>G
ENST00000560467.2:c.1890C>G ENSP00000453513.2:p.Thr630=
ENST00000558518.6:c.2010C>G MANE Select ENSP00000454071.1:p.Thr670=
ENST00000252444.9:c.2264C>G
ENST00000455727.6:c.1506C>G ENSP00000397829.2:p.Thr502=
ENST00000535915.5:c.1887C>G ENSP00000440520.1:p.Thr629=
ENST00000545707.5:c.1606+159C>G ENSP00000437639.1:n.1606+159C>G
ENST00000557933.5:c.2010C>G ENSP00000453557.1:p.Thr670=
ENST00000558013.5:c.2010C>G ENSP00000453346.1:p.Thr670=
ENST00000558518.5:c.2010C>G ENSP00000454071.1:p.Thr670=
ENST00000559340.1:c.591C>G
NM_000527.4:c.2010C>G , LRG_274t1:c.2010C>G NP_000518.1:p.Thr670=
NM_001195798.1:c.2010C>G NP_001182727.1:p.Thr670=
NM_001195799.1:c.1887C>G NP_001182728.1:p.Thr629=
NM_001195800.1:c.1506C>G NP_001182729.1:p.Thr502=
NM_001195803.1:c.1606+159C>G NP_001182732.1:n.1606+159C>G
XM_011528010.1:c.2010C>G XP_011526312.1:p.Thr670=
XM_011528011.1:c.1629C>G XP_011526313.1:p.Thr543=
XR_244074.2:n.2020C>G
XM_011528010.2:c.2010C>G XP_011526312.1:p.Thr670=
XR_001753685.2:n.2127C>G
XR_001753686.2:n.1987C>G
NM_000527.5:c.2010C>G MANE Select NP_000518.1:p.Thr670=
NM_001195798.2:c.2010C>G NP_001182727.1:p.Thr670=
NM_001195799.2:c.1887C>G NP_001182728.1:p.Thr629=
NM_001195800.2:c.1506C>G NP_001182729.1:p.Thr502=
NM_001195803.2:c.1606+159C>G NP_001182732.1:n.1606+159C>G