Canonical Allele Identifier: CA10585672

Gene: LDLR

Linked Data

• ClinVar Variation Id: 252102
• ClinVar RCV Id: RCV000237121 ; RCV001854907
• dbSNP Id: rs875989934
• MyVariant Identifiers: chr19:g.11230802C>T (hg19) ; chr19:g.11120126C>T (hg38)
• PubMed: PMID:9763532

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120126C>T , CM000681.2:g.11120126C>T	GRCh38
NC_000019.9:g.11230802C>T , CM000681.1:g.11230802C>T	GRCh37
NC_000019.8:g.11091802C>T	NCBI36
NG_009060.1:g.35746C>T , LRG_274:g.35746C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2138C>T	ENSP00000252444.6:p.Ala713Val
ENST00000559340.2:c.1740C>T	ENSP00000453696.2:p.Ser580=
ENST00000560467.2:c.1760C>T	ENSP00000453513.2:p.Ala587Val
ENST00000558518.6:c.1880C>T MANE Select	ENSP00000454071.1:p.Ala627Val
ENST00000252444.9:c.2134C>T
ENST00000455727.6:c.1376C>T	ENSP00000397829.2:p.Ala459Val
ENST00000535915.5:c.1757C>T	ENSP00000440520.1:p.Ala586Val
ENST00000545707.5:c.1499C>T	ENSP00000437639.1:p.Ala500Val
ENST00000557933.5:c.1880C>T	ENSP00000453557.1:p.Ala627Val
ENST00000558013.5:c.1880C>T	ENSP00000453346.1:p.Ala627Val
ENST00000558518.5:c.1880C>T	ENSP00000454071.1:p.Ala627Val
ENST00000559340.1:c.461C>T
NM_000527.4:c.1880C>T , LRG_274t1:c.1880C>T	NP_000518.1:p.Ala627Val
NM_001195798.1:c.1880C>T	NP_001182727.1:p.Ala627Val
NM_001195799.1:c.1757C>T	NP_001182728.1:p.Ala586Val
NM_001195800.1:c.1376C>T	NP_001182729.1:p.Ala459Val
NM_001195803.1:c.1499C>T	NP_001182732.1:p.Ala500Val
XM_011528010.1:c.1880C>T	XP_011526312.1:p.Ala627Val
XM_011528011.1:c.1499C>T	XP_011526313.1:p.Ala500Val
XR_244074.2:n.1890C>T
XM_011528010.2:c.1880C>T	XP_011526312.1:p.Ala627Val
XR_001753685.2:n.1997C>T
XR_001753686.2:n.1857C>T
NM_000527.5:c.1880C>T MANE Select	NP_000518.1:p.Ala627Val
NM_001195798.2:c.1880C>T	NP_001182727.1:p.Ala627Val
NM_001195799.2:c.1757C>T	NP_001182728.1:p.Ala586Val
NM_001195800.2:c.1376C>T	NP_001182729.1:p.Ala459Val
NM_001195803.2:c.1499C>T	NP_001182732.1:p.Ala500Val