Canonical Allele Identifier: CA404089817

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11227635A>T (hg19) ; chr19:g.11116959A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11116959A>T , CM000681.2:g.11116959A>T	GRCh38
NC_000019.9:g.11227635A>T , CM000681.1:g.11227635A>T	GRCh37
NC_000019.8:g.11088635A>T	NCBI36
NG_009060.1:g.32579A>T , LRG_274:g.32579A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2064A>T	ENSP00000252444.6:p.Glu688Asp
ENST00000559340.2:c.1705+747A>T	ENSP00000453696.2:n.1705+747A>T
ENST00000560467.2:c.1686A>T	ENSP00000453513.2:p.Glu562Asp
ENST00000558518.6:c.1806A>T MANE Select	ENSP00000454071.1:p.Glu602Asp
ENST00000252444.9:c.2060A>T
ENST00000455727.6:c.1302A>T	ENSP00000397829.2:p.Glu434Asp
ENST00000535915.5:c.1683A>T	ENSP00000440520.1:p.Glu561Asp
ENST00000545707.5:c.1425A>T	ENSP00000437639.1:p.Glu475Asp
ENST00000557933.5:c.1806A>T	ENSP00000453557.1:p.Glu602Asp
ENST00000558013.5:c.1806A>T	ENSP00000453346.1:p.Glu602Asp
ENST00000558518.5:c.1806A>T	ENSP00000454071.1:p.Glu602Asp
ENST00000559340.1:c.426+747A>T
NM_000527.4:c.1806A>T , LRG_274t1:c.1806A>T	NP_000518.1:p.Glu602Asp
NM_001195798.1:c.1806A>T	NP_001182727.1:p.Glu602Asp
NM_001195799.1:c.1683A>T	NP_001182728.1:p.Glu561Asp
NM_001195800.1:c.1302A>T	NP_001182729.1:p.Glu434Asp
NM_001195803.1:c.1425A>T	NP_001182732.1:p.Glu475Asp
XM_011528010.1:c.1806A>T	XP_011526312.1:p.Glu602Asp
XM_011528011.1:c.1425A>T	XP_011526313.1:p.Glu475Asp
XR_244074.2:n.1855+747A>T
XM_011528010.2:c.1806A>T	XP_011526312.1:p.Glu602Asp
XR_001753685.2:n.1923A>T
XR_001753686.2:n.1822+747A>T
NM_000527.5:c.1806A>T MANE Select	NP_000518.1:p.Glu602Asp
NM_001195798.2:c.1806A>T	NP_001182727.1:p.Glu602Asp
NM_001195799.2:c.1683A>T	NP_001182728.1:p.Glu561Asp
NM_001195800.2:c.1302A>T	NP_001182729.1:p.Glu434Asp
NM_001195803.2:c.1425A>T	NP_001182732.1:p.Glu475Asp