Canonical Allele Identifier: CA305302717

Gene: LDLR

Linked Data

• ClinVar Variation Id: 1101468
• ClinVar RCV Id: RCV001424440
• dbSNP Id: rs1031256388
• gnomAD v4: 19-11120389-G-A
• MyVariant Identifiers: chr19:g.11231065G>A (hg19) ; chr19:g.11120389G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120389G>A , CM000681.2:g.11120389G>A	GRCh38
NC_000019.9:g.11231065G>A , CM000681.1:g.11231065G>A	GRCh37
NC_000019.8:g.11092065G>A	NCBI36
NG_009060.1:g.36009G>A , LRG_274:g.36009G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2265G>A	ENSP00000252444.6:p.Arg755=
ENST00000559340.2:c.*76G>A	ENSP00000453696.2:n.*76G>A
ENST00000560467.2:c.1887G>A	ENSP00000453513.2:p.Arg629=
ENST00000558518.6:c.2007G>A MANE Select	ENSP00000454071.1:p.Arg669=
ENST00000252444.9:c.2261G>A
ENST00000455727.6:c.1503G>A	ENSP00000397829.2:p.Arg501=
ENST00000535915.5:c.1884G>A	ENSP00000440520.1:p.Arg628=
ENST00000545707.5:c.1606+156G>A	ENSP00000437639.1:n.1606+156G>A
ENST00000557933.5:c.2007G>A	ENSP00000453557.1:p.Arg669=
ENST00000558013.5:c.2007G>A	ENSP00000453346.1:p.Arg669=
ENST00000558518.5:c.2007G>A	ENSP00000454071.1:p.Arg669=
ENST00000559340.1:c.588G>A
NM_000527.4:c.2007G>A , LRG_274t1:c.2007G>A	NP_000518.1:p.Arg669=
NM_001195798.1:c.2007G>A	NP_001182727.1:p.Arg669=
NM_001195799.1:c.1884G>A	NP_001182728.1:p.Arg628=
NM_001195800.1:c.1503G>A	NP_001182729.1:p.Arg501=
NM_001195803.1:c.1606+156G>A	NP_001182732.1:n.1606+156G>A
XM_011528010.1:c.2007G>A	XP_011526312.1:p.Arg669=
XM_011528011.1:c.1626G>A	XP_011526313.1:p.Arg542=
XR_244074.2:n.2017G>A
XM_011528010.2:c.2007G>A	XP_011526312.1:p.Arg669=
XR_001753685.2:n.2124G>A
XR_001753686.2:n.1984G>A
NM_000527.5:c.2007G>A MANE Select	NP_000518.1:p.Arg669=
NM_001195798.2:c.2007G>A	NP_001182727.1:p.Arg669=
NM_001195799.2:c.1884G>A	NP_001182728.1:p.Arg628=
NM_001195800.2:c.1503G>A	NP_001182729.1:p.Arg501=
NM_001195803.2:c.1606+156G>A	NP_001182732.1:n.1606+156G>A