Canonical Allele Identifier: CA023543
Gene: LDLR HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116144G>A , CM000681.2:g.11116144G>A GRCh38
NC_000019.9:g.11226820G>A , CM000681.1:g.11226820G>A GRCh37
NC_000019.8:g.11087820G>A NCBI36
NG_009060.1:g.31764G>A , LRG_274:g.31764G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1895G>A ENSP00000252444.6:p.Gly632Asp
ENST00000559340.2:c.1637G>A ENSP00000453696.2:p.Gly546Asp
ENST00000560467.2:c.1517G>A ENSP00000453513.2:p.Gly506Asp
ENST00000558518.6:c.1637G>A MANE Select ENSP00000454071.1:p.Gly546Asp
ENST00000252444.9:c.1891G>A
ENST00000455727.6:c.1133G>A ENSP00000397829.2:p.Gly378Asp
ENST00000535915.5:c.1514G>A ENSP00000440520.1:p.Gly505Asp
ENST00000545707.5:c.1256G>A ENSP00000437639.1:p.Gly419Asp
ENST00000557933.5:c.1637G>A ENSP00000453557.1:p.Gly546Asp
ENST00000558013.5:c.1637G>A ENSP00000453346.1:p.Gly546Asp
ENST00000558518.5:c.1637G>A ENSP00000454071.1:p.Gly546Asp
ENST00000559340.1:c.358G>A
NM_000527.4:c.1637G>A , LRG_274t1:c.1637G>A NP_000518.1:p.Gly546Asp
NM_001195798.1:c.1637G>A NP_001182727.1:p.Gly546Asp
NM_001195799.1:c.1514G>A NP_001182728.1:p.Gly505Asp
NM_001195800.1:c.1133G>A NP_001182729.1:p.Gly378Asp
NM_001195803.1:c.1256G>A NP_001182732.1:p.Gly419Asp
XM_011528010.1:c.1637G>A XP_011526312.1:p.Gly546Asp
XM_011528011.1:c.1256G>A XP_011526313.1:p.Gly419Asp
XR_244074.2:n.1787G>A
XM_011528010.2:c.1637G>A XP_011526312.1:p.Gly546Asp
XR_001753685.2:n.1754G>A
XR_001753686.2:n.1754G>A
NM_000527.5:c.1637G>A MANE Select NP_000518.1:p.Gly546Asp
NM_001195798.2:c.1637G>A NP_001182727.1:p.Gly546Asp
NM_001195799.2:c.1514G>A NP_001182728.1:p.Gly505Asp
NM_001195800.2:c.1133G>A NP_001182729.1:p.Gly378Asp
NM_001195803.2:c.1256G>A NP_001182732.1:p.Gly419Asp