Canonical Allele Identifier: CA505743387
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11230806T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120130T>A , CM000681.2:g.11120130T>A GRCh38
NC_000019.9:g.11230806T>A , CM000681.1:g.11230806T>A GRCh37
NC_000019.8:g.11091806T>A NCBI36
NG_009060.1:g.35750T>A , LRG_274:g.35750T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2142T>A ENSP00000252444.6:p.Ile714=
ENST00000559340.2:c.1744T>A ENSP00000453696.2:p.Phe582Ile
ENST00000560467.2:c.1764T>A ENSP00000453513.2:p.Ile588=
ENST00000558518.6:c.1884T>A MANE Select ENSP00000454071.1:p.Ile628=
ENST00000252444.9:c.2138T>A
ENST00000455727.6:c.1380T>A ENSP00000397829.2:p.Ile460=
ENST00000535915.5:c.1761T>A ENSP00000440520.1:p.Ile587=
ENST00000545707.5:c.1503T>A ENSP00000437639.1:p.Ile501=
ENST00000557933.5:c.1884T>A ENSP00000453557.1:p.Ile628=
ENST00000558013.5:c.1884T>A ENSP00000453346.1:p.Ile628=
ENST00000558518.5:c.1884T>A ENSP00000454071.1:p.Ile628=
ENST00000559340.1:c.465T>A
NM_000527.4:c.1884T>A , LRG_274t1:c.1884T>A NP_000518.1:p.Ile628=
NM_001195798.1:c.1884T>A NP_001182727.1:p.Ile628=
NM_001195799.1:c.1761T>A NP_001182728.1:p.Ile587=
NM_001195800.1:c.1380T>A NP_001182729.1:p.Ile460=
NM_001195803.1:c.1503T>A NP_001182732.1:p.Ile501=
XM_011528010.1:c.1884T>A XP_011526312.1:p.Ile628=
XM_011528011.1:c.1503T>A XP_011526313.1:p.Ile501=
XR_244074.2:n.1894T>A
XM_011528010.2:c.1884T>A XP_011526312.1:p.Ile628=
XR_001753685.2:n.2001T>A
XR_001753686.2:n.1861T>A
NM_000527.5:c.1884T>A MANE Select NP_000518.1:p.Ile628=
NM_001195798.2:c.1884T>A NP_001182727.1:p.Ile628=
NM_001195799.2:c.1761T>A NP_001182728.1:p.Ile587=
NM_001195800.2:c.1380T>A NP_001182729.1:p.Ile460=
NM_001195803.2:c.1503T>A NP_001182732.1:p.Ile501=