Canonical Allele Identifier: CA505743395

Gene: LDLR

Linked Data

• ClinVar Variation Id: 2773524
• ClinVar RCV Id: RCV003582123
• dbSNP Id: rs1382517876
• gnomAD v3: 19-11120226-G-A
• gnomAD v4: 19-11120226-G-A
• MyVariant Identifiers: chr19:g.11230902G>A (hg19) ; chr19:g.11120226G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120226G>A , CM000681.2:g.11120226G>A	GRCh38
NC_000019.9:g.11230902G>A , CM000681.1:g.11230902G>A	GRCh37
NC_000019.8:g.11091902G>A	NCBI36
NG_009060.1:g.35846G>A , LRG_274:g.35846G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2238G>A	ENSP00000252444.6:p.Gln746=
ENST00000559340.2:c.*49G>A	ENSP00000453696.2:n.*49G>A
ENST00000560467.2:c.1860G>A	ENSP00000453513.2:p.Gln620=
ENST00000558518.6:c.1980G>A MANE Select	ENSP00000454071.1:p.Gln660=
ENST00000252444.9:c.2234G>A
ENST00000455727.6:c.1476G>A	ENSP00000397829.2:p.Gln492=
ENST00000535915.5:c.1857G>A	ENSP00000440520.1:p.Gln619=
ENST00000545707.5:c.1599G>A	ENSP00000437639.1:p.Gln533=
ENST00000557933.5:c.1980G>A	ENSP00000453557.1:p.Gln660=
ENST00000558013.5:c.1980G>A	ENSP00000453346.1:p.Gln660=
ENST00000558518.5:c.1980G>A	ENSP00000454071.1:p.Gln660=
ENST00000559340.1:c.561G>A
NM_000527.4:c.1980G>A , LRG_274t1:c.1980G>A	NP_000518.1:p.Gln660=
NM_001195798.1:c.1980G>A	NP_001182727.1:p.Gln660=
NM_001195799.1:c.1857G>A	NP_001182728.1:p.Gln619=
NM_001195800.1:c.1476G>A	NP_001182729.1:p.Gln492=
NM_001195803.1:c.1599G>A	NP_001182732.1:p.Gln533=
XM_011528010.1:c.1980G>A	XP_011526312.1:p.Gln660=
XM_011528011.1:c.1599G>A	XP_011526313.1:p.Gln533=
XR_244074.2:n.1990G>A
XM_011528010.2:c.1980G>A	XP_011526312.1:p.Gln660=
XR_001753685.2:n.2097G>A
XR_001753686.2:n.1957G>A
NM_000527.5:c.1980G>A MANE Select	NP_000518.1:p.Gln660=
NM_001195798.2:c.1980G>A	NP_001182727.1:p.Gln660=
NM_001195799.2:c.1857G>A	NP_001182728.1:p.Gln619=
NM_001195800.2:c.1476G>A	NP_001182729.1:p.Gln492=
NM_001195803.2:c.1599G>A	NP_001182732.1:p.Gln533=