Canonical Allele Identifier: CA10585601

Gene: LDLR

Linked Data

• ClinVar Variation Id: 252018
• ClinVar RCV Id: RCV000238270
• dbSNP Id: rs879255012
• gnomAD v4: 19-11116907-T-C
• MyVariant Identifiers: chr19:g.11227583T>C (hg19) ; chr19:g.11116907T>C (hg38)
• PubMed: PMID:17347910

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11116907T>C , CM000681.2:g.11116907T>C	GRCh38
NC_000019.9:g.11227583T>C , CM000681.1:g.11227583T>C	GRCh37
NC_000019.8:g.11088583T>C	NCBI36
NG_009060.1:g.32527T>C , LRG_274:g.32527T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2012T>C	ENSP00000252444.6:p.Ile671Thr
ENST00000559340.2:c.1705+695T>C	ENSP00000453696.2:n.1705+695T>C
ENST00000560467.2:c.1634T>C	ENSP00000453513.2:p.Ile545Thr
ENST00000558518.6:c.1754T>C MANE Select	ENSP00000454071.1:p.Ile585Thr
ENST00000252444.9:c.2008T>C
ENST00000455727.6:c.1250T>C	ENSP00000397829.2:p.Ile417Thr
ENST00000535915.5:c.1631T>C	ENSP00000440520.1:p.Ile544Thr
ENST00000545707.5:c.1373T>C	ENSP00000437639.1:p.Ile458Thr
ENST00000557933.5:c.1754T>C	ENSP00000453557.1:p.Ile585Thr
ENST00000558013.5:c.1754T>C	ENSP00000453346.1:p.Ile585Thr
ENST00000558518.5:c.1754T>C	ENSP00000454071.1:p.Ile585Thr
ENST00000559340.1:c.426+695T>C
NM_000527.4:c.1754T>C , LRG_274t1:c.1754T>C	NP_000518.1:p.Ile585Thr
NM_001195798.1:c.1754T>C	NP_001182727.1:p.Ile585Thr
NM_001195799.1:c.1631T>C	NP_001182728.1:p.Ile544Thr
NM_001195800.1:c.1250T>C	NP_001182729.1:p.Ile417Thr
NM_001195803.1:c.1373T>C	NP_001182732.1:p.Ile458Thr
XM_011528010.1:c.1754T>C	XP_011526312.1:p.Ile585Thr
XM_011528011.1:c.1373T>C	XP_011526313.1:p.Ile458Thr
XR_244074.2:n.1855+695T>C
XM_011528010.2:c.1754T>C	XP_011526312.1:p.Ile585Thr
XR_001753685.2:n.1871T>C
XR_001753686.2:n.1822+695T>C
NM_000527.5:c.1754T>C MANE Select	NP_000518.1:p.Ile585Thr
NM_001195798.2:c.1754T>C	NP_001182727.1:p.Ile585Thr
NM_001195799.2:c.1631T>C	NP_001182728.1:p.Ile544Thr
NM_001195800.2:c.1250T>C	NP_001182729.1:p.Ile417Thr
NM_001195803.2:c.1373T>C	NP_001182732.1:p.Ile458Thr