Canonical Allele Identifier: CA10585286

Gene: LDLR

Linked Data

• ClinVar Variation Id: 251644
• ClinVar RCV Id: RCV000238556
• dbSNP Id: rs767767730
• MyVariant Identifiers: chr19:g.11222195G>C (hg19) ; chr19:g.11111519G>C (hg38)
• PubMed: PMID:15256764 ; PMID:20145306

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11111519G>C , CM000681.2:g.11111519G>C	GRCh38
NC_000019.9:g.11222195G>C , CM000681.1:g.11222195G>C	GRCh37
NC_000019.8:g.11083195G>C	NCBI36
NG_009060.1:g.27139G>C , LRG_274:g.27139G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1324G>C	ENSP00000252444.6:p.Asp442His
ENST00000559340.2:c.1066G>C	ENSP00000453696.2:p.Asp356His
ENST00000560467.2:c.946G>C	ENSP00000453513.2:p.Asp316His
ENST00000558518.6:c.1066G>C MANE Select	ENSP00000454071.1:p.Asp356His
ENST00000252444.9:c.1320G>C
ENST00000455727.6:c.562G>C	ENSP00000397829.2:p.Asp188His
ENST00000535915.5:c.943G>C	ENSP00000440520.1:p.Asp315His
ENST00000545707.5:c.685G>C	ENSP00000437639.1:p.Asp229His
ENST00000557933.5:c.1066G>C	ENSP00000453557.1:p.Asp356His
ENST00000558013.5:c.1066G>C	ENSP00000453346.1:p.Asp356His
ENST00000558518.5:c.1066G>C	ENSP00000454071.1:p.Asp356His
ENST00000560173.1:n.65G>C
ENST00000560467.1:c.546G>C
NM_000527.4:c.1066G>C , LRG_274t1:c.1066G>C	NP_000518.1:p.Asp356His
NM_001195798.1:c.1066G>C	NP_001182727.1:p.Asp356His
NM_001195799.1:c.943G>C	NP_001182728.1:p.Asp315His
NM_001195800.1:c.562G>C	NP_001182729.1:p.Asp188His
NM_001195803.1:c.685G>C	NP_001182732.1:p.Asp229His
XM_011528010.1:c.1066G>C	XP_011526312.1:p.Asp356His
XM_011528011.1:c.685G>C	XP_011526313.1:p.Asp229His
XR_244074.2:n.1216G>C
XM_011528010.2:c.1066G>C	XP_011526312.1:p.Asp356His
XR_001753685.2:n.1183G>C
XR_001753686.2:n.1183G>C
NM_000527.5:c.1066G>C MANE Select	NP_000518.1:p.Asp356His
NM_001195798.2:c.1066G>C	NP_001182727.1:p.Asp356His
NM_001195799.2:c.943G>C	NP_001182728.1:p.Asp315His
NM_001195800.2:c.562G>C	NP_001182729.1:p.Asp188His
NM_001195803.2:c.685G>C	NP_001182732.1:p.Asp229His