Canonical Allele Identifier: CA404082754
Gene: LDLR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11221412A>T (hg19) chr19:g.11110736A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110736A>T , CM000681.2:g.11110736A>T GRCh38
NC_000019.9:g.11221412A>T , CM000681.1:g.11221412A>T GRCh37
NC_000019.8:g.11082412A>T NCBI36
NG_009060.1:g.26356A>T , LRG_274:g.26356A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1283A>T ENSP00000252444.6:p.Asp428Val
ENST00000559340.2:c.1025A>T ENSP00000453696.2:p.Asp342Val
ENST00000560467.2:c.941-778A>T ENSP00000453513.2:n.941-778A>T
ENST00000558518.6:c.1025A>T MANE Select ENSP00000454071.1:p.Asp342Val
ENST00000252444.9:c.1279A>T
ENST00000455727.6:c.521A>T ENSP00000397829.2:p.Asp174Val
ENST00000535915.5:c.902A>T ENSP00000440520.1:p.Asp301Val
ENST00000545707.5:c.644A>T ENSP00000437639.1:p.Asp215Val
ENST00000557933.5:c.1025A>T ENSP00000453557.1:p.Asp342Val
ENST00000558013.5:c.1025A>T ENSP00000453346.1:p.Asp342Val
ENST00000558518.5:c.1025A>T ENSP00000454071.1:p.Asp342Val
ENST00000560173.1:n.24A>T
ENST00000560467.1:c.541-778A>T
NM_000527.4:c.1025A>T , LRG_274t1:c.1025A>T NP_000518.1:p.Asp342Val
NM_001195798.1:c.1025A>T NP_001182727.1:p.Asp342Val
NM_001195799.1:c.902A>T NP_001182728.1:p.Asp301Val
NM_001195800.1:c.521A>T NP_001182729.1:p.Asp174Val
NM_001195803.1:c.644A>T NP_001182732.1:p.Asp215Val
XM_011528010.1:c.1025A>T XP_011526312.1:p.Asp342Val
XM_011528011.1:c.644A>T XP_011526313.1:p.Asp215Val
XR_244074.2:n.1175A>T
XM_011528010.2:c.1025A>T XP_011526312.1:p.Asp342Val
XR_001753685.2:n.1142A>T
XR_001753686.2:n.1142A>T
NM_000527.5:c.1025A>T MANE Select NP_000518.1:p.Asp342Val
NM_001195798.2:c.1025A>T NP_001182727.1:p.Asp342Val
NM_001195799.2:c.902A>T NP_001182728.1:p.Asp301Val
NM_001195800.2:c.521A>T NP_001182729.1:p.Asp174Val
NM_001195803.2:c.644A>T NP_001182732.1:p.Asp215Val
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