Canonical Allele Identifier: CA038535

Gene: LDLR

Linked Data

• ClinVar Variation Id: 990077
• ClinVar RCV Id: RCV001278019 ; RCV002418871 ; RCV004004939
• dbSNP Id: rs370835628
• ExAC: 19:11231155 G / A
• gnomAD v2: 19-11231155-G-A
• gnomAD v3: 19-11120479-G-A
• gnomAD v4: 19-11120479-G-A
• MyVariant Identifiers: chr19:g.11231155G>A (hg19) ; chr19:g.11120479G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120479G>A , CM000681.2:g.11120479G>A	GRCh38
NC_000019.9:g.11231155G>A , CM000681.1:g.11231155G>A	GRCh37
NC_000019.8:g.11092155G>A	NCBI36
NG_009060.1:g.36099G>A , LRG_274:g.36099G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2355G>A	ENSP00000252444.6:p.Pro785=
ENST00000559340.2:c.*166G>A	ENSP00000453696.2:n.*166G>A
ENST00000560467.2:c.1977G>A	ENSP00000453513.2:p.Pro659=
ENST00000558518.6:c.2097G>A MANE Select	ENSP00000454071.1:p.Pro699=
ENST00000252444.9:c.2351G>A
ENST00000455727.6:c.1593G>A	ENSP00000397829.2:p.Pro531=
ENST00000535915.5:c.1974G>A	ENSP00000440520.1:p.Pro658=
ENST00000545707.5:c.1606+246G>A	ENSP00000437639.1:n.1606+246G>A
ENST00000557933.5:c.2097G>A	ENSP00000453557.1:p.Pro699=
ENST00000558013.5:c.2097G>A	ENSP00000453346.1:p.Pro699=
ENST00000558518.5:c.2097G>A	ENSP00000454071.1:p.Pro699=
NM_000527.4:c.2097G>A , LRG_274t1:c.2097G>A	NP_000518.1:p.Pro699=
NM_001195798.1:c.2097G>A	NP_001182727.1:p.Pro699=
NM_001195799.1:c.1974G>A	NP_001182728.1:p.Pro658=
NM_001195800.1:c.1593G>A	NP_001182729.1:p.Pro531=
NM_001195803.1:c.1606+246G>A	NP_001182732.1:n.1606+246G>A
XM_011528010.1:c.2097G>A	XP_011526312.1:p.Pro699=
XM_011528011.1:c.1716G>A	XP_011526313.1:p.Pro572=
XR_244074.2:n.2107G>A
XM_011528010.2:c.2097G>A	XP_011526312.1:p.Pro699=
XR_001753685.2:n.2214G>A
XR_001753686.2:n.2074G>A
NM_000527.5:c.2097G>A MANE Select	NP_000518.1:p.Pro699=
NM_001195798.2:c.2097G>A	NP_001182727.1:p.Pro699=
NM_001195799.2:c.1974G>A	NP_001182728.1:p.Pro658=
NM_001195800.2:c.1593G>A	NP_001182729.1:p.Pro531=
NM_001195803.2:c.1606+246G>A	NP_001182732.1:n.1606+246G>A