Canonical Allele Identifier: CA505486875
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11233878G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123202G>A , CM000681.2:g.11123202G>A GRCh38
NC_000019.9:g.11233878G>A , CM000681.1:g.11233878G>A GRCh37
NC_000019.8:g.11094878G>A NCBI36
NG_009060.1:g.38822G>A , LRG_274:g.38822G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2427G>A ENSP00000252444.6:p.Glu809=
ENST00000559340.2:c.*238G>A ENSP00000453696.2:n.*238G>A
ENST00000560467.2:c.2049G>A ENSP00000453513.2:p.Glu683=
ENST00000558518.6:c.2169G>A MANE Select ENSP00000454071.1:p.Glu723=
ENST00000252444.9:c.2423G>A
ENST00000455727.6:c.1665G>A ENSP00000397829.2:p.Glu555=
ENST00000535915.5:c.2046G>A ENSP00000440520.1:p.Glu682=
ENST00000545707.5:c.1635G>A ENSP00000437639.1:p.Glu545=
ENST00000557933.5:c.2169G>A ENSP00000453557.1:p.Glu723=
ENST00000558013.5:c.2169G>A ENSP00000453346.1:p.Glu723=
ENST00000558518.5:c.2169G>A ENSP00000454071.1:p.Glu723=
NM_000527.4:c.2169G>A , LRG_274t1:c.2169G>A NP_000518.1:p.Glu723=
NM_001195798.1:c.2169G>A NP_001182727.1:p.Glu723=
NM_001195799.1:c.2046G>A NP_001182728.1:p.Glu682=
NM_001195800.1:c.1665G>A NP_001182729.1:p.Glu555=
NM_001195803.1:c.1635G>A NP_001182732.1:p.Glu545=
XM_011528010.1:c.2169G>A XP_011526312.1:p.Glu723=
XM_011528011.1:c.1788G>A XP_011526313.1:p.Glu596=
XR_244074.2:n.2179G>A
XM_011528010.2:c.2169G>A XP_011526312.1:p.Glu723=
XR_001753685.2:n.2503G>A
XR_001753686.2:n.2146G>A
NM_000527.5:c.2169G>A MANE Select NP_000518.1:p.Glu723=
NM_001195798.2:c.2169G>A NP_001182727.1:p.Glu723=
NM_001195799.2:c.2046G>A NP_001182728.1:p.Glu682=
NM_001195800.2:c.1665G>A NP_001182729.1:p.Glu555=
NM_001195803.2:c.1635G>A NP_001182732.1:p.Glu545=