Canonical Allele Identifier: CA404086451

Gene: LDLR

Linked Data

• ClinVar Variation Id: 977992
• ClinVar RCV Id: RCV001255948
• dbSNP Id: rs2077419716
• MyVariant Identifiers: chr19:g.11224353G>A (hg19) ; chr19:g.11113677G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113677G>A , CM000681.2:g.11113677G>A	GRCh38
NC_000019.9:g.11224353G>A , CM000681.1:g.11224353G>A	GRCh37
NC_000019.8:g.11085353G>A	NCBI36
NG_009060.1:g.29297G>A , LRG_274:g.29297G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1759G>A	ENSP00000252444.6:p.Ala587Thr
ENST00000559340.2:c.1501G>A	ENSP00000453696.2:p.Ala501Thr
ENST00000560467.2:c.1381G>A	ENSP00000453513.2:p.Ala461Thr
ENST00000558518.6:c.1501G>A MANE Select	ENSP00000454071.1:p.Ala501Thr
ENST00000252444.9:c.1755G>A
ENST00000455727.6:c.997G>A	ENSP00000397829.2:p.Ala333Thr
ENST00000535915.5:c.1378G>A	ENSP00000440520.1:p.Ala460Thr
ENST00000545707.5:c.1120G>A	ENSP00000437639.1:p.Ala374Thr
ENST00000557933.5:c.1501G>A	ENSP00000453557.1:p.Ala501Thr
ENST00000558013.5:c.1501G>A	ENSP00000453346.1:p.Ala501Thr
ENST00000558518.5:c.1501G>A	ENSP00000454071.1:p.Ala501Thr
ENST00000559340.1:c.222G>A
NM_000527.4:c.1501G>A , LRG_274t1:c.1501G>A	NP_000518.1:p.Ala501Thr
NM_001195798.1:c.1501G>A	NP_001182727.1:p.Ala501Thr
NM_001195799.1:c.1378G>A	NP_001182728.1:p.Ala460Thr
NM_001195800.1:c.997G>A	NP_001182729.1:p.Ala333Thr
NM_001195803.1:c.1120G>A	NP_001182732.1:p.Ala374Thr
XM_011528010.1:c.1501G>A	XP_011526312.1:p.Ala501Thr
XM_011528011.1:c.1120G>A	XP_011526313.1:p.Ala374Thr
XR_244074.2:n.1651G>A
XM_011528010.2:c.1501G>A	XP_011526312.1:p.Ala501Thr
XR_001753685.2:n.1618G>A
XR_001753686.2:n.1618G>A
NM_000527.5:c.1501G>A MANE Select	NP_000518.1:p.Ala501Thr
NM_001195798.2:c.1501G>A	NP_001182727.1:p.Ala501Thr
NM_001195799.2:c.1378G>A	NP_001182728.1:p.Ala460Thr
NM_001195800.2:c.997G>A	NP_001182729.1:p.Ala333Thr
NM_001195803.2:c.1120G>A	NP_001182732.1:p.Ala374Thr