Canonical Allele Identifier: CA505485375
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11221398G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110722G>A , CM000681.2:g.11110722G>A GRCh38
NC_000019.9:g.11221398G>A , CM000681.1:g.11221398G>A GRCh37
NC_000019.8:g.11082398G>A NCBI36
NG_009060.1:g.26342G>A , LRG_274:g.26342G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1269G>A ENSP00000252444.6:p.Glu423=
ENST00000559340.2:c.1011G>A ENSP00000453696.2:p.Glu337=
ENST00000560467.2:c.941-792G>A ENSP00000453513.2:n.941-792G>A
ENST00000558518.6:c.1011G>A MANE Select ENSP00000454071.1:p.Glu337=
ENST00000252444.9:c.1265G>A
ENST00000455727.6:c.507G>A ENSP00000397829.2:p.Glu169=
ENST00000535915.5:c.888G>A ENSP00000440520.1:p.Glu296=
ENST00000545707.5:c.630G>A ENSP00000437639.1:p.Glu210=
ENST00000557933.5:c.1011G>A ENSP00000453557.1:p.Glu337=
ENST00000558013.5:c.1011G>A ENSP00000453346.1:p.Glu337=
ENST00000558518.5:c.1011G>A ENSP00000454071.1:p.Glu337=
ENST00000560173.1:n.10G>A
ENST00000560467.1:c.541-792G>A
NM_000527.4:c.1011G>A , LRG_274t1:c.1011G>A NP_000518.1:p.Glu337=
NM_001195798.1:c.1011G>A NP_001182727.1:p.Glu337=
NM_001195799.1:c.888G>A NP_001182728.1:p.Glu296=
NM_001195800.1:c.507G>A NP_001182729.1:p.Glu169=
NM_001195803.1:c.630G>A NP_001182732.1:p.Glu210=
XM_011528010.1:c.1011G>A XP_011526312.1:p.Glu337=
XM_011528011.1:c.630G>A XP_011526313.1:p.Glu210=
XR_244074.2:n.1161G>A
XM_011528010.2:c.1011G>A XP_011526312.1:p.Glu337=
XR_001753685.2:n.1128G>A
XR_001753686.2:n.1128G>A
NM_000527.5:c.1011G>A MANE Select NP_000518.1:p.Glu337=
NM_001195798.2:c.1011G>A NP_001182727.1:p.Glu337=
NM_001195799.2:c.888G>A NP_001182728.1:p.Glu296=
NM_001195800.2:c.507G>A NP_001182729.1:p.Glu169=
NM_001195803.2:c.630G>A NP_001182732.1:p.Glu210=