Canonical Allele Identifier: CA023426
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 183138
dbSNP Id: rs11669576

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11111624G>A , CM000681.2:g.11111624G>A GRCh38
NC_000019.9:g.11222300G>A , CM000681.1:g.11222300G>A GRCh37
NC_000019.8:g.11083300G>A NCBI36
NG_009060.1:g.27244G>A , LRG_274:g.27244G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1429G>A ENSP00000252444.6:p.Ala477Thr
ENST00000559340.2:c.1171G>A ENSP00000453696.2:p.Ala391Thr
ENST00000560467.2:c.1051G>A ENSP00000453513.2:p.Ala351Thr
ENST00000558518.6:c.1171G>A MANE Select ENSP00000454071.1:p.Ala391Thr
ENST00000252444.9:c.1425G>A
ENST00000455727.6:c.667G>A ENSP00000397829.2:p.Ala223Thr
ENST00000535915.5:c.1048G>A ENSP00000440520.1:p.Ala350Thr
ENST00000545707.5:c.790G>A ENSP00000437639.1:p.Ala264Thr
ENST00000557933.5:c.1171G>A ENSP00000453557.1:p.Ala391Thr
ENST00000558013.5:c.1171G>A ENSP00000453346.1:p.Ala391Thr
ENST00000558518.5:c.1171G>A ENSP00000454071.1:p.Ala391Thr
ENST00000560173.1:n.170G>A
ENST00000560467.1:c.651G>A
NM_000527.4:c.1171G>A , LRG_274t1:c.1171G>A NP_000518.1:p.Ala391Thr
NM_001195798.1:c.1171G>A NP_001182727.1:p.Ala391Thr
NM_001195799.1:c.1048G>A NP_001182728.1:p.Ala350Thr
NM_001195800.1:c.667G>A NP_001182729.1:p.Ala223Thr
NM_001195803.1:c.790G>A NP_001182732.1:p.Ala264Thr
XM_011528010.1:c.1171G>A XP_011526312.1:p.Ala391Thr
XM_011528011.1:c.790G>A XP_011526313.1:p.Ala264Thr
XR_244074.2:n.1321G>A
XM_011528010.2:c.1171G>A XP_011526312.1:p.Ala391Thr
XR_001753685.2:n.1288G>A
XR_001753686.2:n.1288G>A
NM_000527.5:c.1171G>A MANE Select NP_000518.1:p.Ala391Thr
NM_001195798.2:c.1171G>A NP_001182727.1:p.Ala391Thr
NM_001195799.2:c.1048G>A NP_001182728.1:p.Ala350Thr
NM_001195800.2:c.667G>A NP_001182729.1:p.Ala223Thr
NM_001195803.2:c.790G>A NP_001182732.1:p.Ala264Thr