Canonical Allele Identifier: CA404086111

Gene: LDLR

Linked Data

• ClinVar Variation Id: 1345847
• ClinVar RCV Id: RCV002037595
• dbSNP Id: rs2147248832
• MyVariant Identifiers: chr19:g.11224302A>G (hg19) ; chr19:g.11113626A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113626A>G , CM000681.2:g.11113626A>G	GRCh38
NC_000019.9:g.11224302A>G , CM000681.1:g.11224302A>G	GRCh37
NC_000019.8:g.11085302A>G	NCBI36
NG_009060.1:g.29246A>G , LRG_274:g.29246A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1708A>G	ENSP00000252444.6:p.Ile570Val
ENST00000559340.2:c.1450A>G	ENSP00000453696.2:p.Ile484Val
ENST00000560467.2:c.1330A>G	ENSP00000453513.2:p.Ile444Val
ENST00000558518.6:c.1450A>G MANE Select	ENSP00000454071.1:p.Ile484Val
ENST00000252444.9:c.1704A>G
ENST00000455727.6:c.946A>G	ENSP00000397829.2:p.Ile316Val
ENST00000535915.5:c.1327A>G	ENSP00000440520.1:p.Ile443Val
ENST00000545707.5:c.1069A>G	ENSP00000437639.1:p.Ile357Val
ENST00000557933.5:c.1450A>G	ENSP00000453557.1:p.Ile484Val
ENST00000558013.5:c.1450A>G	ENSP00000453346.1:p.Ile484Val
ENST00000558518.5:c.1450A>G	ENSP00000454071.1:p.Ile484Val
ENST00000559340.1:c.171A>G
NM_000527.4:c.1450A>G , LRG_274t1:c.1450A>G	NP_000518.1:p.Ile484Val
NM_001195798.1:c.1450A>G	NP_001182727.1:p.Ile484Val
NM_001195799.1:c.1327A>G	NP_001182728.1:p.Ile443Val
NM_001195800.1:c.946A>G	NP_001182729.1:p.Ile316Val
NM_001195803.1:c.1069A>G	NP_001182732.1:p.Ile357Val
XM_011528010.1:c.1450A>G	XP_011526312.1:p.Ile484Val
XM_011528011.1:c.1069A>G	XP_011526313.1:p.Ile357Val
XR_244074.2:n.1600A>G
XM_011528010.2:c.1450A>G	XP_011526312.1:p.Ile484Val
XR_001753685.2:n.1567A>G
XR_001753686.2:n.1567A>G
NM_000527.5:c.1450A>G MANE Select	NP_000518.1:p.Ile484Val
NM_001195798.2:c.1450A>G	NP_001182727.1:p.Ile484Val
NM_001195799.2:c.1327A>G	NP_001182728.1:p.Ile443Val
NM_001195800.2:c.946A>G	NP_001182729.1:p.Ile316Val
NM_001195803.2:c.1069A>G	NP_001182732.1:p.Ile357Val