Canonical Allele Identifier: CA2576625871

Gene: LDLR

Linked Data

• ClinVar Variation Id: 2783481
• ClinVar RCV Id: RCV003741425
• gnomAD v4: 19-11106547-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11106547C>G , CM000681.2:g.11106547C>G	GRCh38
NC_000019.9:g.11217223C>G , CM000681.1:g.11217223C>G	GRCh37
NC_000019.8:g.11078223C>G	NCBI36
NG_009060.1:g.22167C>G , LRG_274:g.22167C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.953-18C>G	ENSP00000252444.6:n.953-18C>G
ENST00000559340.2:c.695-18C>G	ENSP00000453696.2:n.695-18C>G
ENST00000560467.2:c.695-18C>G	ENSP00000453513.2:n.695-18C>G
ENST00000558518.6:c.695-18C>G MANE Select	ENSP00000454071.1:n.695-18C>G
ENST00000252444.9:c.949-18C>G
ENST00000455727.6:c.314-845C>G	ENSP00000397829.2:n.314-845C>G
ENST00000535915.5:c.572-18C>G	ENSP00000440520.1:n.572-18C>G
ENST00000545707.5:c.314-18C>G	ENSP00000437639.1:n.314-18C>G
ENST00000557933.5:c.695-18C>G	ENSP00000453557.1:n.695-18C>G
ENST00000558013.5:c.695-18C>G	ENSP00000453346.1:n.695-18C>G
ENST00000558518.5:c.695-18C>G	ENSP00000454071.1:n.695-18C>G
ENST00000558528.1:n.192C>G
ENST00000560467.1:c.295-18C>G
NM_000527.4:c.695-18C>G , LRG_274t1:c.695-18C>G	NP_000518.1:n.695-18C>G
NM_001195798.1:c.695-18C>G	NP_001182727.1:n.695-18C>G
NM_001195799.1:c.572-18C>G	NP_001182728.1:n.572-18C>G
NM_001195800.1:c.314-845C>G	NP_001182729.1:n.314-845C>G
NM_001195803.1:c.314-18C>G	NP_001182732.1:n.314-18C>G
XM_011528010.1:c.695-18C>G	XP_011526312.1:n.695-18C>G
XM_011528011.1:c.314-18C>G	XP_011526313.1:n.314-18C>G
XR_244074.2:n.845-18C>G
XM_011528010.2:c.695-18C>G	XP_011526312.1:n.695-18C>G
XR_001753685.2:n.812-18C>G
XR_001753686.2:n.812-18C>G
NM_000527.5:c.695-18C>G MANE Select	NP_000518.1:n.695-18C>G
NM_001195798.2:c.695-18C>G	NP_001182727.1:n.695-18C>G
NM_001195799.2:c.572-18C>G	NP_001182728.1:n.572-18C>G
NM_001195800.2:c.314-845C>G	NP_001182729.1:n.314-845C>G
NM_001195803.2:c.314-18C>G	NP_001182732.1:n.314-18C>G