Canonical Allele Identifier: CA10585258
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251606
dbSNP Id: rs879254760

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110739G>A , CM000681.2:g.11110739G>A GRCh38
NC_000019.9:g.11221415G>A , CM000681.1:g.11221415G>A GRCh37
NC_000019.8:g.11082415G>A NCBI36
NG_009060.1:g.26359G>A , LRG_274:g.26359G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1286G>A ENSP00000252444.6:p.Gly429Asp
ENST00000559340.2:c.1028G>A ENSP00000453696.2:p.Gly343Asp
ENST00000560467.2:c.941-775G>A ENSP00000453513.2:n.941-775G>A
ENST00000558518.6:c.1028G>A MANE Select ENSP00000454071.1:p.Gly343Asp
ENST00000252444.9:c.1282G>A
ENST00000455727.6:c.524G>A ENSP00000397829.2:p.Gly175Asp
ENST00000535915.5:c.905G>A ENSP00000440520.1:p.Gly302Asp
ENST00000545707.5:c.647G>A ENSP00000437639.1:p.Gly216Asp
ENST00000557933.5:c.1028G>A ENSP00000453557.1:p.Gly343Asp
ENST00000558013.5:c.1028G>A ENSP00000453346.1:p.Gly343Asp
ENST00000558518.5:c.1028G>A ENSP00000454071.1:p.Gly343Asp
ENST00000560173.1:n.27G>A
ENST00000560467.1:c.541-775G>A
NM_000527.4:c.1028G>A , LRG_274t1:c.1028G>A NP_000518.1:p.Gly343Asp
NM_001195798.1:c.1028G>A NP_001182727.1:p.Gly343Asp
NM_001195799.1:c.905G>A NP_001182728.1:p.Gly302Asp
NM_001195800.1:c.524G>A NP_001182729.1:p.Gly175Asp
NM_001195803.1:c.647G>A NP_001182732.1:p.Gly216Asp
XM_011528010.1:c.1028G>A XP_011526312.1:p.Gly343Asp
XM_011528011.1:c.647G>A XP_011526313.1:p.Gly216Asp
XR_244074.2:n.1178G>A
XM_011528010.2:c.1028G>A XP_011526312.1:p.Gly343Asp
XR_001753685.2:n.1145G>A
XR_001753686.2:n.1145G>A
NM_000527.5:c.1028G>A MANE Select NP_000518.1:p.Gly343Asp
NM_001195798.2:c.1028G>A NP_001182727.1:p.Gly343Asp
NM_001195799.2:c.905G>A NP_001182728.1:p.Gly302Asp
NM_001195800.2:c.524G>A NP_001182729.1:p.Gly175Asp
NM_001195803.2:c.647G>A NP_001182732.1:p.Gly216Asp