Canonical Allele Identifier: CA10585577

Gene: LDLR

Linked Data

• ClinVar Variation Id: 251987
• ClinVar RCV Id: RCV000238389
• dbSNP Id: rs878854027
• MyVariant Identifiers: chr19:g.11227533A>C (hg19) ; chr19:g.11116857A>C (hg38)
• PubMed: PMID:19318025

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11116857A>C , CM000681.2:g.11116857A>C	GRCh38
NC_000019.9:g.11227533A>C , CM000681.1:g.11227533A>C	GRCh37
NC_000019.8:g.11088533A>C	NCBI36
NG_009060.1:g.32477A>C , LRG_274:g.32477A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1964-2A>C	ENSP00000252444.6:n.1964-2A>C
ENST00000559340.2:c.1705+645A>C	ENSP00000453696.2:n.1705+645A>C
ENST00000560467.2:c.1586-2A>C	ENSP00000453513.2:n.1586-2A>C
ENST00000558518.6:c.1706-2A>C MANE Select	ENSP00000454071.1:n.1706-2A>C
ENST00000252444.9:c.1960-2A>C
ENST00000455727.6:c.1202-2A>C	ENSP00000397829.2:n.1202-2A>C
ENST00000535915.5:c.1583-2A>C	ENSP00000440520.1:n.1583-2A>C
ENST00000545707.5:c.1325-2A>C	ENSP00000437639.1:n.1325-2A>C
ENST00000557933.5:c.1706-2A>C	ENSP00000453557.1:n.1706-2A>C
ENST00000558013.5:c.1706-2A>C	ENSP00000453346.1:n.1706-2A>C
ENST00000558518.5:c.1706-2A>C	ENSP00000454071.1:n.1706-2A>C
ENST00000559340.1:c.426+645A>C
NM_000527.4:c.1706-2A>C , LRG_274t1:c.1706-2A>C	NP_000518.1:n.1706-2A>C
NM_001195798.1:c.1706-2A>C	NP_001182727.1:n.1706-2A>C
NM_001195799.1:c.1583-2A>C	NP_001182728.1:n.1583-2A>C
NM_001195800.1:c.1202-2A>C	NP_001182729.1:n.1202-2A>C
NM_001195803.1:c.1325-2A>C	NP_001182732.1:n.1325-2A>C
XM_011528010.1:c.1706-2A>C	XP_011526312.1:n.1706-2A>C
XM_011528011.1:c.1325-2A>C	XP_011526313.1:n.1325-2A>C
XR_244074.2:n.1855+645A>C
XM_011528010.2:c.1706-2A>C	XP_011526312.1:n.1706-2A>C
XR_001753685.2:n.1823-2A>C
XR_001753686.2:n.1822+645A>C
NM_000527.5:c.1706-2A>C MANE Select	NP_000518.1:n.1706-2A>C
NM_001195798.2:c.1706-2A>C	NP_001182727.1:n.1706-2A>C
NM_001195799.2:c.1583-2A>C	NP_001182728.1:n.1583-2A>C
NM_001195800.2:c.1202-2A>C	NP_001182729.1:n.1202-2A>C
NM_001195803.2:c.1325-2A>C	NP_001182732.1:n.1325-2A>C