Canonical Allele Identifier: CA2582476228

Gene: LDLR

Linked Data

• gnomAD v4: 19-11127932-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11127932C>A , CM000681.2:g.11127932C>A	GRCh38
NC_000019.9:g.11238608C>A , CM000681.1:g.11238608C>A	GRCh37
NC_000019.8:g.11099608C>A	NCBI36
NG_009060.1:g.43552C>A , LRG_274:g.43552C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2570-76C>A	ENSP00000252444.6:n.2570-76C>A
ENST00000559340.2:c.*381-76C>A	ENSP00000453696.2:n.*381-76C>A
ENST00000560467.2:c.2192-76C>A	ENSP00000453513.2:n.2192-76C>A
ENST00000558518.6:c.2312-76C>A MANE Select	ENSP00000454071.1:n.2312-76C>A
ENST00000252444.9:c.2566-76C>A
ENST00000455727.6:c.1808-76C>A	ENSP00000397829.2:n.1808-76C>A
ENST00000535915.5:c.2189-76C>A	ENSP00000440520.1:n.2189-76C>A
ENST00000545707.5:c.1778-76C>A	ENSP00000437639.1:n.1778-76C>A
ENST00000557933.5:c.2312-76C>A	ENSP00000453557.1:n.2312-76C>A
ENST00000558013.5:c.2312-76C>A	ENSP00000453346.1:n.2312-76C>A
ENST00000558518.5:c.2312-76C>A	ENSP00000454071.1:n.2312-76C>A
ENST00000560628.1:n.108+278C>A
NM_000527.4:c.2312-76C>A , LRG_274t1:c.2312-76C>A	NP_000518.1:n.2312-76C>A
NM_001195798.1:c.2312-76C>A	NP_001182727.1:n.2312-76C>A
NM_001195799.1:c.2189-76C>A	NP_001182728.1:n.2189-76C>A
NM_001195800.1:c.1808-76C>A	NP_001182729.1:n.1808-76C>A
NM_001195803.1:c.1778-76C>A	NP_001182732.1:n.1778-76C>A
XM_011528010.1:c.2312-1581C>A	XP_011526312.1:n.2312-1581C>A
XM_011528011.1:c.1931-76C>A	XP_011526313.1:n.1931-76C>A
XR_244074.2:n.2322-76C>A
XM_011528010.2:c.2312-1581C>A	XP_011526312.1:n.2312-1581C>A
XR_001753685.2:n.2646-76C>A
XR_001753686.2:n.2289-76C>A
NM_000527.5:c.2312-76C>A MANE Select	NP_000518.1:n.2312-76C>A
NM_001195798.2:c.2312-76C>A	NP_001182727.1:n.2312-76C>A
NM_001195799.2:c.2189-76C>A	NP_001182728.1:n.2189-76C>A
NM_001195800.2:c.1808-76C>A	NP_001182729.1:n.1808-76C>A
NM_001195803.2:c.1778-76C>A	NP_001182732.1:n.1778-76C>A