Canonical Allele Identifier: CA404095729
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 920005
ClinVar RCV Id: RCV001178496
dbSNP Id: rs759440817

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123324T>G , CM000681.2:g.11123324T>G GRCh38
NC_000019.9:g.11234000T>G , CM000681.1:g.11234000T>G GRCh37
NC_000019.8:g.11095000T>G NCBI36
NG_009060.1:g.38944T>G , LRG_274:g.38944T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2549T>G ENSP00000252444.6:p.Ile850Arg
ENST00000559340.2:c.*360T>G ENSP00000453696.2:n.*360T>G
ENST00000560467.2:c.2171T>G ENSP00000453513.2:p.Ile724Arg
ENST00000558518.6:c.2291T>G MANE Select ENSP00000454071.1:p.Ile764Arg
ENST00000252444.9:c.2545T>G
ENST00000455727.6:c.1787T>G ENSP00000397829.2:p.Ile596Arg
ENST00000535915.5:c.2168T>G ENSP00000440520.1:p.Ile723Arg
ENST00000545707.5:c.1757T>G ENSP00000437639.1:p.Ile586Arg
ENST00000557933.5:c.2291T>G ENSP00000453557.1:p.Ile764Arg
ENST00000558013.5:c.2291T>G ENSP00000453346.1:p.Ile764Arg
ENST00000558518.5:c.2291T>G ENSP00000454071.1:p.Ile764Arg
NM_000527.4:c.2291T>G , LRG_274t1:c.2291T>G NP_000518.1:p.Ile764Arg
NM_001195798.1:c.2291T>G NP_001182727.1:p.Ile764Arg
NM_001195799.1:c.2168T>G NP_001182728.1:p.Ile723Arg
NM_001195800.1:c.1787T>G NP_001182729.1:p.Ile596Arg
NM_001195803.1:c.1757T>G NP_001182732.1:p.Ile586Arg
XM_011528010.1:c.2291T>G XP_011526312.1:p.Ile764Arg
XM_011528011.1:c.1910T>G XP_011526313.1:p.Ile637Arg
XR_244074.2:n.2301T>G
XM_011528010.2:c.2291T>G XP_011526312.1:p.Ile764Arg
XR_001753685.2:n.2625T>G
XR_001753686.2:n.2268T>G
NM_000527.5:c.2291T>G MANE Select NP_000518.1:p.Ile764Arg
NM_001195798.2:c.2291T>G NP_001182727.1:p.Ile764Arg
NM_001195799.2:c.2168T>G NP_001182728.1:p.Ile723Arg
NM_001195800.2:c.1787T>G NP_001182729.1:p.Ile596Arg
NM_001195803.2:c.1757T>G NP_001182732.1:p.Ile586Arg