Canonical Allele Identifier: CA2322777203
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123234C= , CM000681.2:g.11123234C= GRCh38
NC_000019.9:g.11233910C= , CM000681.1:g.11233910C= GRCh37
NC_000019.8:g.11094910C= NCBI36
NG_009060.1:g.38854C= , LRG_274:g.38854C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2459C= ENSP00000252444.6:p.Thr820=
ENST00000559340.2:c.*270C= ENSP00000453696.2:n.*270C=
ENST00000560467.2:c.2081C= ENSP00000453513.2:p.Thr694=
ENST00000558518.6:c.2201C= MANE Select ENSP00000454071.1:p.Thr734=
ENST00000252444.9:c.2455C=
ENST00000455727.6:c.1697C= ENSP00000397829.2:p.Thr566=
ENST00000535915.5:c.2078C= ENSP00000440520.1:p.Thr693=
ENST00000545707.5:c.1667C= ENSP00000437639.1:p.Thr556=
ENST00000557933.5:c.2201C= ENSP00000453557.1:p.Thr734=
ENST00000558013.5:c.2201C= ENSP00000453346.1:p.Thr734=
ENST00000558518.5:c.2201C= ENSP00000454071.1:p.Thr734=
NM_000527.4:c.2201C= , LRG_274t1:c.2201C= NP_000518.1:p.Thr734=
NM_001195798.1:c.2201C= NP_001182727.1:p.Thr734=
NM_001195799.1:c.2078C= NP_001182728.1:p.Thr693=
NM_001195800.1:c.1697C= NP_001182729.1:p.Thr566=
NM_001195803.1:c.1667C= NP_001182732.1:p.Thr556=
XM_011528010.1:c.2201C= XP_011526312.1:p.Thr734=
XM_011528011.1:c.1820C= XP_011526313.1:p.Thr607=
XR_244074.2:n.2211C=
XM_011528010.2:c.2201C= XP_011526312.1:p.Thr734=
XR_001753685.2:n.2535C=
XR_001753686.2:n.2178C=
NM_000527.5:c.2201C= MANE Select NP_000518.1:p.Thr734=
NM_001195798.2:c.2201C= NP_001182727.1:p.Thr734=
NM_001195799.2:c.2078C= NP_001182728.1:p.Thr693=
NM_001195800.2:c.1697C= NP_001182729.1:p.Thr566=
NM_001195803.2:c.1667C= NP_001182732.1:p.Thr556=