Canonical Allele Identifier: CA10585695

Gene: LDLR

Linked Data

• ClinVar Variation Id: 252129
• ClinVar RCV Id: RCV000238503 ; RCV001854909
• dbSNP Id: rs879255085
• MyVariant Identifiers: chr19:g.11230879G>T (hg19) ; chr19:g.11120203G>T (hg38)
• PubMed: PMID:14974088

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120203G>T , CM000681.2:g.11120203G>T	GRCh38
NC_000019.9:g.11230879G>T , CM000681.1:g.11230879G>T	GRCh37
NC_000019.8:g.11091879G>T	NCBI36
NG_009060.1:g.35823G>T , LRG_274:g.35823G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2215G>T	ENSP00000252444.6:p.Val739Phe
ENST00000559340.2:c.*26G>T	ENSP00000453696.2:n.*26G>T
ENST00000560467.2:c.1837G>T	ENSP00000453513.2:p.Val613Phe
ENST00000558518.6:c.1957G>T MANE Select	ENSP00000454071.1:p.Val653Phe
ENST00000252444.9:c.2211G>T
ENST00000455727.6:c.1453G>T	ENSP00000397829.2:p.Val485Phe
ENST00000535915.5:c.1834G>T	ENSP00000440520.1:p.Val612Phe
ENST00000545707.5:c.1576G>T	ENSP00000437639.1:p.Val526Phe
ENST00000557933.5:c.1957G>T	ENSP00000453557.1:p.Val653Phe
ENST00000558013.5:c.1957G>T	ENSP00000453346.1:p.Val653Phe
ENST00000558518.5:c.1957G>T	ENSP00000454071.1:p.Val653Phe
ENST00000559340.1:c.538G>T
NM_000527.4:c.1957G>T , LRG_274t1:c.1957G>T	NP_000518.1:p.Val653Phe
NM_001195798.1:c.1957G>T	NP_001182727.1:p.Val653Phe
NM_001195799.1:c.1834G>T	NP_001182728.1:p.Val612Phe
NM_001195800.1:c.1453G>T	NP_001182729.1:p.Val485Phe
NM_001195803.1:c.1576G>T	NP_001182732.1:p.Val526Phe
XM_011528010.1:c.1957G>T	XP_011526312.1:p.Val653Phe
XM_011528011.1:c.1576G>T	XP_011526313.1:p.Val526Phe
XR_244074.2:n.1967G>T
XM_011528010.2:c.1957G>T	XP_011526312.1:p.Val653Phe
XR_001753685.2:n.2074G>T
XR_001753686.2:n.1934G>T
NM_000527.5:c.1957G>T MANE Select	NP_000518.1:p.Val653Phe
NM_001195798.2:c.1957G>T	NP_001182727.1:p.Val653Phe
NM_001195799.2:c.1834G>T	NP_001182728.1:p.Val612Phe
NM_001195800.2:c.1453G>T	NP_001182729.1:p.Val485Phe
NM_001195803.2:c.1576G>T	NP_001182732.1:p.Val526Phe