Canonical Allele Identifier: CA10585162

Gene: LDLR

Linked Data

• ClinVar Variation Id: 251489
• ClinVar RCV Id: RCV000238295 ; RCV001043441
• dbSNP Id: rs375495026
• MyVariant Identifiers: chr19:g.11218109G>T (hg19) ; chr19:g.11107433G>T (hg38)
• ERepo: CA10585162/MONDO:0007750/013
• PubMed: PMID:12730724 ; PMID:17196209

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107433G>T , CM000681.2:g.11107433G>T	GRCh38
NC_000019.9:g.11218109G>T , CM000681.1:g.11218109G>T	GRCh37
NC_000019.8:g.11079109G>T	NCBI36
NG_009060.1:g.23053G>T , LRG_274:g.23053G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1117G>T	ENSP00000252444.6:p.Gly373Cys
ENST00000559340.2:c.859G>T	ENSP00000453696.2:p.Gly287Cys
ENST00000560467.2:c.859G>T	ENSP00000453513.2:p.Gly287Cys
ENST00000558518.6:c.859G>T MANE Select	ENSP00000454071.1:p.Gly287Cys
ENST00000252444.9:c.1113G>T
ENST00000455727.6:c.355G>T	ENSP00000397829.2:p.Gly119Cys
ENST00000535915.5:c.736G>T	ENSP00000440520.1:p.Gly246Cys
ENST00000545707.5:c.478G>T	ENSP00000437639.1:p.Gly160Cys
ENST00000557933.5:c.859G>T	ENSP00000453557.1:p.Gly287Cys
ENST00000558013.5:c.859G>T	ENSP00000453346.1:p.Gly287Cys
ENST00000558518.5:c.859G>T	ENSP00000454071.1:p.Gly287Cys
ENST00000558528.1:n.374G>T
ENST00000560467.1:c.459G>T
NM_000527.4:c.859G>T , LRG_274t1:c.859G>T	NP_000518.1:p.Gly287Cys
NM_001195798.1:c.859G>T	NP_001182727.1:p.Gly287Cys
NM_001195799.1:c.736G>T	NP_001182728.1:p.Gly246Cys
NM_001195800.1:c.355G>T	NP_001182729.1:p.Gly119Cys
NM_001195803.1:c.478G>T	NP_001182732.1:p.Gly160Cys
XM_011528010.1:c.859G>T	XP_011526312.1:p.Gly287Cys
XM_011528011.1:c.478G>T	XP_011526313.1:p.Gly160Cys
XR_244074.2:n.1009G>T
XM_011528010.2:c.859G>T	XP_011526312.1:p.Gly287Cys
XR_001753685.2:n.976G>T
XR_001753686.2:n.976G>T
NM_000527.5:c.859G>T MANE Select	NP_000518.1:p.Gly287Cys
NM_001195798.2:c.859G>T	NP_001182727.1:p.Gly287Cys
NM_001195799.2:c.736G>T	NP_001182728.1:p.Gly246Cys
NM_001195800.2:c.355G>T	NP_001182729.1:p.Gly119Cys
NM_001195803.2:c.478G>T	NP_001182732.1:p.Gly160Cys