Canonical Allele Identifier: CA2582473460

Gene: LDLR

Linked Data

• gnomAD v4: 19-11105334-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11105337dup , CM000681.2:g.11105337dup	GRCh38
NC_000019.9:g.11216013dup , CM000681.1:g.11216013dup	GRCh37
NC_000019.8:g.11077013dup	NCBI36
NG_009060.1:g.20957dup , LRG_274:g.20957dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.689dup	ENSP00000252444.6:p.Val231GlyfsTer?
ENST00000559340.2:c.431dup	ENSP00000453696.2:p.Val145GlyfsTer?
ENST00000560467.2:c.431dup	ENSP00000453513.2:p.Val145GlyfsTer?
ENST00000558518.6:c.431dup MANE Select	ENSP00000454071.1:p.Val145GlyfsTer?
ENST00000252444.9:c.685dup
ENST00000455727.6:c.314-2055dup	ENSP00000397829.2:n.314-2055dup
ENST00000535915.5:c.308dup	ENSP00000440520.1:p.Val104GlyfsTer?
ENST00000545707.5:c.314-1228dup	ENSP00000437639.1:n.314-1228dup
ENST00000557933.5:c.431dup	ENSP00000453557.1:p.Val145GlyfsTer?
ENST00000558013.5:c.431dup	ENSP00000453346.1:p.Val145GlyfsTer?
ENST00000558518.5:c.431dup	ENSP00000454071.1:p.Val145GlyfsTer?
ENST00000560467.1:c.31dup
NM_000527.4:c.431dup , LRG_274t1:c.431dup	NP_000518.1:p.Val145GlyfsTer?
NM_001195798.1:c.431dup	NP_001182727.1:p.Val145GlyfsTer?
NM_001195799.1:c.308dup	NP_001182728.1:p.Val104GlyfsTer?
NM_001195800.1:c.314-2055dup	NP_001182729.1:n.314-2055dup
NM_001195803.1:c.314-1228dup	NP_001182732.1:n.314-1228dup
XM_011528010.1:c.431dup	XP_011526312.1:p.Val145GlyfsTer?
XM_011528011.1:c.314-1228dup	XP_011526313.1:n.314-1228dup
XR_244074.2:n.581dup
XM_011528010.2:c.431dup	XP_011526312.1:p.Val145GlyfsTer?
XR_001753685.2:n.548dup
XR_001753686.2:n.548dup
NM_000527.5:c.431dup MANE Select	NP_000518.1:p.Val145GlyfsTer?
NM_001195798.2:c.431dup	NP_001182727.1:p.Val145GlyfsTer?
NM_001195799.2:c.308dup	NP_001182728.1:p.Val104GlyfsTer?
NM_001195800.2:c.314-2055dup	NP_001182729.1:n.314-2055dup
NM_001195803.2:c.314-1228dup	NP_001182732.1:n.314-1228dup