Canonical Allele Identifier: CA10576307

Gene: LDLR

Linked Data

• ClinVar Variation Id: 226357
• ClinVar RCV Id: RCV000211689 ; RCV001389977
• dbSNP Id: rs875989922
• MyVariant Identifiers: chr19:g.11224321G>A (hg19) ; chr19:g.11113645G>A (hg38)
• PubMed: PMID:8103503 ; PMID:22881376

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113645G>A , CM000681.2:g.11113645G>A	GRCh38
NC_000019.9:g.11224321G>A , CM000681.1:g.11224321G>A	GRCh37
NC_000019.8:g.11085321G>A	NCBI36
NG_009060.1:g.29265G>A , LRG_274:g.29265G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1727G>A	ENSP00000252444.6:p.Trp576Ter
ENST00000559340.2:c.1469G>A	ENSP00000453696.2:p.Trp490Ter
ENST00000560467.2:c.1349G>A	ENSP00000453513.2:p.Trp450Ter
ENST00000558518.6:c.1469G>A MANE Select	ENSP00000454071.1:p.Trp490Ter
ENST00000252444.9:c.1723G>A
ENST00000455727.6:c.965G>A	ENSP00000397829.2:p.Trp322Ter
ENST00000535915.5:c.1346G>A	ENSP00000440520.1:p.Trp449Ter
ENST00000545707.5:c.1088G>A	ENSP00000437639.1:p.Trp363Ter
ENST00000557933.5:c.1469G>A	ENSP00000453557.1:p.Trp490Ter
ENST00000558013.5:c.1469G>A	ENSP00000453346.1:p.Trp490Ter
ENST00000558518.5:c.1469G>A	ENSP00000454071.1:p.Trp490Ter
ENST00000559340.1:c.190G>A
NM_000527.4:c.1469G>A , LRG_274t1:c.1469G>A	NP_000518.1:p.Trp490Ter
NM_001195798.1:c.1469G>A	NP_001182727.1:p.Trp490Ter
NM_001195799.1:c.1346G>A	NP_001182728.1:p.Trp449Ter
NM_001195800.1:c.965G>A	NP_001182729.1:p.Trp322Ter
NM_001195803.1:c.1088G>A	NP_001182732.1:p.Trp363Ter
XM_011528010.1:c.1469G>A	XP_011526312.1:p.Trp490Ter
XM_011528011.1:c.1088G>A	XP_011526313.1:p.Trp363Ter
XR_244074.2:n.1619G>A
XM_011528010.2:c.1469G>A	XP_011526312.1:p.Trp490Ter
XR_001753685.2:n.1586G>A
XR_001753686.2:n.1586G>A
NM_000527.5:c.1469G>A MANE Select	NP_000518.1:p.Trp490Ter
NM_001195798.2:c.1469G>A	NP_001182727.1:p.Trp490Ter
NM_001195799.2:c.1346G>A	NP_001182728.1:p.Trp449Ter
NM_001195800.2:c.965G>A	NP_001182729.1:p.Trp322Ter
NM_001195803.2:c.1088G>A	NP_001182732.1:p.Trp363Ter