Canonical Allele Identifier: CA10585702

Gene: LDLR

Linked Data

• ClinVar Variation Id: 252138
• ClinVar RCV Id: RCV000237122
• dbSNP Id: rs879255092
• MyVariant Identifiers: chr19:g.11230895T>C (hg19) ; chr19:g.11120219T>C (hg38)
• PubMed: PMID:20809525

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120219T>C , CM000681.2:g.11120219T>C	GRCh38
NC_000019.9:g.11230895T>C , CM000681.1:g.11230895T>C	GRCh37
NC_000019.8:g.11091895T>C	NCBI36
NG_009060.1:g.35839T>C , LRG_274:g.35839T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2231T>C	ENSP00000252444.6:p.Leu744Pro
ENST00000559340.2:c.*42T>C	ENSP00000453696.2:n.*42T>C
ENST00000560467.2:c.1853T>C	ENSP00000453513.2:p.Leu618Pro
ENST00000558518.6:c.1973T>C MANE Select	ENSP00000454071.1:p.Leu658Pro
ENST00000252444.9:c.2227T>C
ENST00000455727.6:c.1469T>C	ENSP00000397829.2:p.Leu490Pro
ENST00000535915.5:c.1850T>C	ENSP00000440520.1:p.Leu617Pro
ENST00000545707.5:c.1592T>C	ENSP00000437639.1:p.Leu531Pro
ENST00000557933.5:c.1973T>C	ENSP00000453557.1:p.Leu658Pro
ENST00000558013.5:c.1973T>C	ENSP00000453346.1:p.Leu658Pro
ENST00000558518.5:c.1973T>C	ENSP00000454071.1:p.Leu658Pro
ENST00000559340.1:c.554T>C
NM_000527.4:c.1973T>C , LRG_274t1:c.1973T>C	NP_000518.1:p.Leu658Pro
NM_001195798.1:c.1973T>C	NP_001182727.1:p.Leu658Pro
NM_001195799.1:c.1850T>C	NP_001182728.1:p.Leu617Pro
NM_001195800.1:c.1469T>C	NP_001182729.1:p.Leu490Pro
NM_001195803.1:c.1592T>C	NP_001182732.1:p.Leu531Pro
XM_011528010.1:c.1973T>C	XP_011526312.1:p.Leu658Pro
XM_011528011.1:c.1592T>C	XP_011526313.1:p.Leu531Pro
XR_244074.2:n.1983T>C
XM_011528010.2:c.1973T>C	XP_011526312.1:p.Leu658Pro
XR_001753685.2:n.2090T>C
XR_001753686.2:n.1950T>C
NM_000527.5:c.1973T>C MANE Select	NP_000518.1:p.Leu658Pro
NM_001195798.2:c.1973T>C	NP_001182727.1:p.Leu658Pro
NM_001195799.2:c.1850T>C	NP_001182728.1:p.Leu617Pro
NM_001195800.2:c.1469T>C	NP_001182729.1:p.Leu490Pro
NM_001195803.2:c.1592T>C	NP_001182732.1:p.Leu531Pro