Canonical Allele Identifier: CA2322775623
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120468T= , CM000681.2:g.11120468T= GRCh38
NC_000019.9:g.11231144T= , CM000681.1:g.11231144T= GRCh37
NC_000019.8:g.11092144T= NCBI36
NG_009060.1:g.36088T= , LRG_274:g.36088T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2344T= ENSP00000252444.6:p.Cys782=
ENST00000559340.2:c.*155T= ENSP00000453696.2:n.*155T=
ENST00000560467.2:c.1966T= ENSP00000453513.2:p.Cys656=
ENST00000558518.6:c.2086T= MANE Select ENSP00000454071.1:p.Cys696=
ENST00000252444.9:c.2340T=
ENST00000455727.6:c.1582T= ENSP00000397829.2:p.Cys528=
ENST00000535915.5:c.1963T= ENSP00000440520.1:p.Cys655=
ENST00000545707.5:c.1606+235T= ENSP00000437639.1:n.1606+235T=
ENST00000557933.5:c.2086T= ENSP00000453557.1:p.Cys696=
ENST00000558013.5:c.2086T= ENSP00000453346.1:p.Cys696=
ENST00000558518.5:c.2086T= ENSP00000454071.1:p.Cys696=
NM_000527.4:c.2086T= , LRG_274t1:c.2086T= NP_000518.1:p.Cys696=
NM_001195798.1:c.2086T= NP_001182727.1:p.Cys696=
NM_001195799.1:c.1963T= NP_001182728.1:p.Cys655=
NM_001195800.1:c.1582T= NP_001182729.1:p.Cys528=
NM_001195803.1:c.1606+235T= NP_001182732.1:n.1606+235T=
XM_011528010.1:c.2086T= XP_011526312.1:p.Cys696=
XM_011528011.1:c.1705T= XP_011526313.1:p.Cys569=
XR_244074.2:n.2096T=
XM_011528010.2:c.2086T= XP_011526312.1:p.Cys696=
XR_001753685.2:n.2203T=
XR_001753686.2:n.2063T=
NM_000527.5:c.2086T= MANE Select NP_000518.1:p.Cys696=
NM_001195798.2:c.2086T= NP_001182727.1:p.Cys696=
NM_001195799.2:c.1963T= NP_001182728.1:p.Cys655=
NM_001195800.2:c.1582T= NP_001182729.1:p.Cys528=
NM_001195803.2:c.1606+235T= NP_001182732.1:n.1606+235T=