Canonical Allele Identifier: CA023635
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 183130
dbSNP Id: rs368838866

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120483G>A , CM000681.2:g.11120483G>A GRCh38
NC_000019.9:g.11231159G>A , CM000681.1:g.11231159G>A GRCh37
NC_000019.8:g.11092159G>A NCBI36
NG_009060.1:g.36103G>A , LRG_274:g.36103G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2359G>A ENSP00000252444.6:p.Gly787Ser
ENST00000559340.2:c.*170G>A ENSP00000453696.2:n.*170G>A
ENST00000560467.2:c.1981G>A ENSP00000453513.2:p.Gly661Ser
ENST00000558518.6:c.2101G>A MANE Select ENSP00000454071.1:p.Gly701Ser
ENST00000252444.9:c.2355G>A
ENST00000455727.6:c.1597G>A ENSP00000397829.2:p.Gly533Ser
ENST00000535915.5:c.1978G>A ENSP00000440520.1:p.Gly660Ser
ENST00000545707.5:c.1606+250G>A ENSP00000437639.1:n.1606+250G>A
ENST00000557933.5:c.2101G>A ENSP00000453557.1:p.Gly701Ser
ENST00000558013.5:c.2101G>A ENSP00000453346.1:p.Gly701Ser
ENST00000558518.5:c.2101G>A ENSP00000454071.1:p.Gly701Ser
NM_000527.4:c.2101G>A , LRG_274t1:c.2101G>A NP_000518.1:p.Gly701Ser
NM_001195798.1:c.2101G>A NP_001182727.1:p.Gly701Ser
NM_001195799.1:c.1978G>A NP_001182728.1:p.Gly660Ser
NM_001195800.1:c.1597G>A NP_001182729.1:p.Gly533Ser
NM_001195803.1:c.1606+250G>A NP_001182732.1:n.1606+250G>A
XM_011528010.1:c.2101G>A XP_011526312.1:p.Gly701Ser
XM_011528011.1:c.1720G>A XP_011526313.1:p.Gly574Ser
XR_244074.2:n.2111G>A
XM_011528010.2:c.2101G>A XP_011526312.1:p.Gly701Ser
XR_001753685.2:n.2218G>A
XR_001753686.2:n.2078G>A
NM_000527.5:c.2101G>A MANE Select NP_000518.1:p.Gly701Ser
NM_001195798.2:c.2101G>A NP_001182727.1:p.Gly701Ser
NM_001195799.2:c.1978G>A NP_001182728.1:p.Gly660Ser
NM_001195800.2:c.1597G>A NP_001182729.1:p.Gly533Ser
NM_001195803.2:c.1606+250G>A NP_001182732.1:n.1606+250G>A