Canonical Allele Identifier: CA10585747

Gene: LDLR

Linked Data

• ClinVar Variation Id: 252193
• ClinVar RCV Id: RCV000238125
• dbSNP Id: rs2569548
• MyVariant Identifiers: chr19:g.11231111C>A (hg19) ; chr19:g.11120435C>A (hg38)
• PubMed: PMID:11810272

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120435C>A , CM000681.2:g.11120435C>A	GRCh38
NC_000019.9:g.11231111C>A , CM000681.1:g.11231111C>A	GRCh37
NC_000019.8:g.11092111C>A	NCBI36
NG_009060.1:g.36055C>A , LRG_274:g.36055C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2311C>A	ENSP00000252444.6:p.Pro771Thr
ENST00000559340.2:c.*122C>A	ENSP00000453696.2:n.*122C>A
ENST00000560467.2:c.1933C>A	ENSP00000453513.2:p.Pro645Thr
ENST00000558518.6:c.2053C>A MANE Select	ENSP00000454071.1:p.Pro685Thr
ENST00000252444.9:c.2307C>A
ENST00000455727.6:c.1549C>A	ENSP00000397829.2:p.Pro517Thr
ENST00000535915.5:c.1930C>A	ENSP00000440520.1:p.Pro644Thr
ENST00000545707.5:c.1606+202C>A	ENSP00000437639.1:n.1606+202C>A
ENST00000557933.5:c.2053C>A	ENSP00000453557.1:p.Pro685Thr
ENST00000558013.5:c.2053C>A	ENSP00000453346.1:p.Pro685Thr
ENST00000558518.5:c.2053C>A	ENSP00000454071.1:p.Pro685Thr
NM_000527.4:c.2053C>A , LRG_274t1:c.2053C>A	NP_000518.1:p.Pro685Thr
NM_001195798.1:c.2053C>A	NP_001182727.1:p.Pro685Thr
NM_001195799.1:c.1930C>A	NP_001182728.1:p.Pro644Thr
NM_001195800.1:c.1549C>A	NP_001182729.1:p.Pro517Thr
NM_001195803.1:c.1606+202C>A	NP_001182732.1:n.1606+202C>A
XM_011528010.1:c.2053C>A	XP_011526312.1:p.Pro685Thr
XM_011528011.1:c.1672C>A	XP_011526313.1:p.Pro558Thr
XR_244074.2:n.2063C>A
XM_011528010.2:c.2053C>A	XP_011526312.1:p.Pro685Thr
XR_001753685.2:n.2170C>A
XR_001753686.2:n.2030C>A
NM_000527.5:c.2053C>A MANE Select	NP_000518.1:p.Pro685Thr
NM_001195798.2:c.2053C>A	NP_001182727.1:p.Pro685Thr
NM_001195799.2:c.1930C>A	NP_001182728.1:p.Pro644Thr
NM_001195800.2:c.1549C>A	NP_001182729.1:p.Pro517Thr
NM_001195803.2:c.1606+202C>A	NP_001182732.1:n.1606+202C>A