Canonical Allele Identifier: CA404099968
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129667C>T , CM000681.2:g.11129667C>T GRCh38
NC_000019.9:g.11240343C>T , CM000681.1:g.11240343C>T GRCh37
NC_000019.8:g.11101343C>T NCBI36
NG_009060.1:g.45287C>T , LRG_274:g.45287C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2802C>T ENSP00000252444.6:p.Pro934=
ENST00000559340.2:c.*613C>T ENSP00000453696.2:n.*613C>T
ENST00000560467.2:c.2424C>T ENSP00000453513.2:p.Pro808=
ENST00000558518.6:c.2544C>T MANE Select ENSP00000454071.1:p.Pro848=
ENST00000252444.9:c.2798C>T
ENST00000455727.6:c.2040C>T ENSP00000397829.2:p.Pro680=
ENST00000535915.5:c.2421C>T ENSP00000440520.1:p.Pro807=
ENST00000545707.5:c.2010C>T ENSP00000437639.1:p.Pro670=
ENST00000557933.5:c.2606C>T ENSP00000453557.1:p.Pro869Leu
ENST00000558013.5:c.2544C>T ENSP00000453346.1:p.Pro848=
ENST00000558518.5:c.2544C>T ENSP00000454071.1:p.Pro848=
ENST00000560628.1:n.108+2013C>T
NM_000527.4:c.2544C>T , LRG_274t1:c.2544C>T NP_000518.1:p.Pro848=
NM_001195798.1:c.2544C>T NP_001182727.1:p.Pro848=
NM_001195799.1:c.2421C>T NP_001182728.1:p.Pro807=
NM_001195800.1:c.2040C>T NP_001182729.1:p.Pro680=
NM_001195803.1:c.2010C>T NP_001182732.1:p.Pro670=
XM_011528010.1:c.2466C>T XP_011526312.1:p.Pro822=
XM_011528011.1:c.2163C>T XP_011526313.1:p.Pro721=
XM_011528010.2:c.2466C>T XP_011526312.1:p.Pro822=
XR_001753685.2:n.2878C>T
XR_001753686.2:n.2521C>T
NM_000527.5:c.2544C>T MANE Select NP_000518.1:p.Pro848=
NM_001195798.2:c.2544C>T NP_001182727.1:p.Pro848=
NM_001195799.2:c.2421C>T NP_001182728.1:p.Pro807=
NM_001195800.2:c.2040C>T NP_001182729.1:p.Pro680=
NM_001195803.2:c.2010C>T NP_001182732.1:p.Pro670=