Canonical Allele Identifier: CA10585403

Gene: LDLR

Linked Data

• ClinVar Variation Id: 251786
• ClinVar RCV Id: RCV002379062
• dbSNP Id: rs879254863
• MyVariant Identifiers: chr19:g.11224091T>C (hg19) ; chr19:g.11113415T>C (hg38)
• PubMed: PMID:17347910

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113415T>C , CM000681.2:g.11113415T>C	GRCh38
NC_000019.9:g.11224091T>C , CM000681.1:g.11224091T>C	GRCh37
NC_000019.8:g.11085091T>C	NCBI36
NG_009060.1:g.29035T>C , LRG_274:g.29035T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1582T>C	ENSP00000252444.6:p.Tyr528His
ENST00000559340.2:c.1324T>C	ENSP00000453696.2:p.Tyr442His
ENST00000560467.2:c.1204T>C	ENSP00000453513.2:p.Tyr402His
ENST00000558518.6:c.1324T>C MANE Select	ENSP00000454071.1:p.Tyr442His
ENST00000252444.9:c.1578T>C
ENST00000455727.6:c.820T>C	ENSP00000397829.2:p.Tyr274His
ENST00000535915.5:c.1201T>C	ENSP00000440520.1:p.Tyr401His
ENST00000545707.5:c.943T>C	ENSP00000437639.1:p.Tyr315His
ENST00000557933.5:c.1324T>C	ENSP00000453557.1:p.Tyr442His
ENST00000558013.5:c.1324T>C	ENSP00000453346.1:p.Tyr442His
ENST00000558518.5:c.1324T>C	ENSP00000454071.1:p.Tyr442His
ENST00000559340.1:c.45T>C
ENST00000560173.1:n.323T>C
ENST00000560467.1:c.804T>C
NM_000527.4:c.1324T>C , LRG_274t1:c.1324T>C	NP_000518.1:p.Tyr442His
NM_001195798.1:c.1324T>C	NP_001182727.1:p.Tyr442His
NM_001195799.1:c.1201T>C	NP_001182728.1:p.Tyr401His
NM_001195800.1:c.820T>C	NP_001182729.1:p.Tyr274His
NM_001195803.1:c.943T>C	NP_001182732.1:p.Tyr315His
XM_011528010.1:c.1324T>C	XP_011526312.1:p.Tyr442His
XM_011528011.1:c.943T>C	XP_011526313.1:p.Tyr315His
XR_244074.2:n.1474T>C
XM_011528010.2:c.1324T>C	XP_011526312.1:p.Tyr442His
XR_001753685.2:n.1441T>C
XR_001753686.2:n.1441T>C
NM_000527.5:c.1324T>C MANE Select	NP_000518.1:p.Tyr442His
NM_001195798.2:c.1324T>C	NP_001182727.1:p.Tyr442His
NM_001195799.2:c.1201T>C	NP_001182728.1:p.Tyr401His
NM_001195800.2:c.820T>C	NP_001182729.1:p.Tyr274His
NM_001195803.2:c.943T>C	NP_001182732.1:p.Tyr315His