Canonical Allele Identifier: CA10584959

Gene: LDLR

Linked Data

• ClinVar Variation Id: 251268
• ClinVar RCV Id: RCV000238056
• dbSNP Id: rs879254554
• gnomAD v4: 19-11105420-G-T
• MyVariant Identifiers: chr19:g.11216096G>T (hg19) ; chr19:g.11105420G>T (hg38)
• PubMed: PMID:11194025 ; PMID:20599862

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11105420G>T , CM000681.2:g.11105420G>T	GRCh38
NC_000019.9:g.11216096G>T , CM000681.1:g.11216096G>T	GRCh37
NC_000019.8:g.11077096G>T	NCBI36
NG_009060.1:g.21040G>T , LRG_274:g.21040G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.772G>T	ENSP00000252444.6:p.Asp258Tyr
ENST00000559340.2:c.514G>T	ENSP00000453696.2:p.Asp172Tyr
ENST00000560467.2:c.514G>T	ENSP00000453513.2:p.Asp172Tyr
ENST00000558518.6:c.514G>T MANE Select	ENSP00000454071.1:p.Asp172Tyr
ENST00000252444.9:c.768G>T
ENST00000455727.6:c.314-1972G>T	ENSP00000397829.2:n.314-1972G>T
ENST00000535915.5:c.391G>T	ENSP00000440520.1:p.Asp131Tyr
ENST00000545707.5:c.314-1145G>T	ENSP00000437639.1:n.314-1145G>T
ENST00000557933.5:c.514G>T	ENSP00000453557.1:p.Asp172Tyr
ENST00000558013.5:c.514G>T	ENSP00000453346.1:p.Asp172Tyr
ENST00000558518.5:c.514G>T	ENSP00000454071.1:p.Asp172Tyr
ENST00000560467.1:c.114G>T
NM_000527.4:c.514G>T , LRG_274t1:c.514G>T	NP_000518.1:p.Asp172Tyr
NM_001195798.1:c.514G>T	NP_001182727.1:p.Asp172Tyr
NM_001195799.1:c.391G>T	NP_001182728.1:p.Asp131Tyr
NM_001195800.1:c.314-1972G>T	NP_001182729.1:n.314-1972G>T
NM_001195803.1:c.314-1145G>T	NP_001182732.1:n.314-1145G>T
XM_011528010.1:c.514G>T	XP_011526312.1:p.Asp172Tyr
XM_011528011.1:c.314-1145G>T	XP_011526313.1:n.314-1145G>T
XR_244074.2:n.664G>T
XM_011528010.2:c.514G>T	XP_011526312.1:p.Asp172Tyr
XR_001753685.2:n.631G>T
XR_001753686.2:n.631G>T
NM_000527.5:c.514G>T MANE Select	NP_000518.1:p.Asp172Tyr
NM_001195798.2:c.514G>T	NP_001182727.1:p.Asp172Tyr
NM_001195799.2:c.391G>T	NP_001182728.1:p.Asp131Tyr
NM_001195800.2:c.314-1972G>T	NP_001182729.1:n.314-1972G>T
NM_001195803.2:c.314-1145G>T	NP_001182732.1:n.314-1145G>T