Canonical Allele Identifier: CA505743268

Gene: LDLR

Linked Data

• ClinVar Variation Id: 2850503
• ClinVar RCV Id: RCV003742173
• MyVariant Identifiers: chr19:g.11224111G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113435G>A , CM000681.2:g.11113435G>A	GRCh38
NC_000019.9:g.11224111G>A , CM000681.1:g.11224111G>A	GRCh37
NC_000019.8:g.11085111G>A	NCBI36
NG_009060.1:g.29055G>A , LRG_274:g.29055G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1602G>A	ENSP00000252444.6:p.Gln534=
ENST00000559340.2:c.1344G>A	ENSP00000453696.2:p.Gln448=
ENST00000560467.2:c.1224G>A	ENSP00000453513.2:p.Gln408=
ENST00000558518.6:c.1344G>A MANE Select	ENSP00000454071.1:p.Gln448=
ENST00000252444.9:c.1598G>A
ENST00000455727.6:c.840G>A	ENSP00000397829.2:p.Gln280=
ENST00000535915.5:c.1221G>A	ENSP00000440520.1:p.Gln407=
ENST00000545707.5:c.963G>A	ENSP00000437639.1:p.Gln321=
ENST00000557933.5:c.1344G>A	ENSP00000453557.1:p.Gln448=
ENST00000558013.5:c.1344G>A	ENSP00000453346.1:p.Gln448=
ENST00000558518.5:c.1344G>A	ENSP00000454071.1:p.Gln448=
ENST00000559340.1:c.65G>A
ENST00000560173.1:n.343G>A
ENST00000560467.1:c.824G>A
NM_000527.4:c.1344G>A , LRG_274t1:c.1344G>A	NP_000518.1:p.Gln448=
NM_001195798.1:c.1344G>A	NP_001182727.1:p.Gln448=
NM_001195799.1:c.1221G>A	NP_001182728.1:p.Gln407=
NM_001195800.1:c.840G>A	NP_001182729.1:p.Gln280=
NM_001195803.1:c.963G>A	NP_001182732.1:p.Gln321=
XM_011528010.1:c.1344G>A	XP_011526312.1:p.Gln448=
XM_011528011.1:c.963G>A	XP_011526313.1:p.Gln321=
XR_244074.2:n.1494G>A
XM_011528010.2:c.1344G>A	XP_011526312.1:p.Gln448=
XR_001753685.2:n.1461G>A
XR_001753686.2:n.1461G>A
NM_000527.5:c.1344G>A MANE Select	NP_000518.1:p.Gln448=
NM_001195798.2:c.1344G>A	NP_001182727.1:p.Gln448=
NM_001195799.2:c.1221G>A	NP_001182728.1:p.Gln407=
NM_001195800.2:c.840G>A	NP_001182729.1:p.Gln280=
NM_001195803.2:c.963G>A	NP_001182732.1:p.Gln321=