Canonical Allele Identifier: CA10585795
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 252244
ClinVar RCV Id: RCV000237109
dbSNP Id: rs879255152

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123197C>T , CM000681.2:g.11123197C>T GRCh38
NC_000019.9:g.11233873C>T , CM000681.1:g.11233873C>T GRCh37
NC_000019.8:g.11094873C>T NCBI36
NG_009060.1:g.38817C>T , LRG_274:g.38817C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2422C>T ENSP00000252444.6:p.Gln808Ter
ENST00000559340.2:c.*233C>T ENSP00000453696.2:n.*233C>T
ENST00000560467.2:c.2044C>T ENSP00000453513.2:p.Gln682Ter
ENST00000558518.6:c.2164C>T MANE Select ENSP00000454071.1:p.Gln722Ter
ENST00000252444.9:c.2418C>T
ENST00000455727.6:c.1660C>T ENSP00000397829.2:p.Gln554Ter
ENST00000535915.5:c.2041C>T ENSP00000440520.1:p.Gln681Ter
ENST00000545707.5:c.1630C>T ENSP00000437639.1:p.Gln544Ter
ENST00000557933.5:c.2164C>T ENSP00000453557.1:p.Gln722Ter
ENST00000558013.5:c.2164C>T ENSP00000453346.1:p.Gln722Ter
ENST00000558518.5:c.2164C>T ENSP00000454071.1:p.Gln722Ter
NM_000527.4:c.2164C>T , LRG_274t1:c.2164C>T NP_000518.1:p.Gln722Ter
NM_001195798.1:c.2164C>T NP_001182727.1:p.Gln722Ter
NM_001195799.1:c.2041C>T NP_001182728.1:p.Gln681Ter
NM_001195800.1:c.1660C>T NP_001182729.1:p.Gln554Ter
NM_001195803.1:c.1630C>T NP_001182732.1:p.Gln544Ter
XM_011528010.1:c.2164C>T XP_011526312.1:p.Gln722Ter
XM_011528011.1:c.1783C>T XP_011526313.1:p.Gln595Ter
XR_244074.2:n.2174C>T
XM_011528010.2:c.2164C>T XP_011526312.1:p.Gln722Ter
XR_001753685.2:n.2498C>T
XR_001753686.2:n.2141C>T
NM_000527.5:c.2164C>T MANE Select NP_000518.1:p.Gln722Ter
NM_001195798.2:c.2164C>T NP_001182727.1:p.Gln722Ter
NM_001195799.2:c.2041C>T NP_001182728.1:p.Gln681Ter
NM_001195800.2:c.1660C>T NP_001182729.1:p.Gln554Ter
NM_001195803.2:c.1630C>T NP_001182732.1:p.Gln544Ter