Canonical Allele Identifier: CA2322770251
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110695C= , CM000681.2:g.11110695C= GRCh38
NC_000019.9:g.11221371C= , CM000681.1:g.11221371C= GRCh37
NC_000019.8:g.11082371C= NCBI36
NG_009060.1:g.26315C= , LRG_274:g.26315C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1242C= ENSP00000252444.6:p.Val414=
ENST00000559340.2:c.984C= ENSP00000453696.2:p.Val328=
ENST00000560467.2:c.941-819C= ENSP00000453513.2:n.941-819C=
ENST00000558518.6:c.984C= MANE Select ENSP00000454071.1:p.Val328=
ENST00000252444.9:c.1238C=
ENST00000455727.6:c.480C= ENSP00000397829.2:p.Val160=
ENST00000535915.5:c.861C= ENSP00000440520.1:p.Val287=
ENST00000545707.5:c.603C= ENSP00000437639.1:p.Val201=
ENST00000557933.5:c.984C= ENSP00000453557.1:p.Val328=
ENST00000558013.5:c.984C= ENSP00000453346.1:p.Val328=
ENST00000558518.5:c.984C= ENSP00000454071.1:p.Val328=
ENST00000560467.1:c.541-819C=
NM_000527.4:c.984C= , LRG_274t1:c.984C= NP_000518.1:p.Val328=
NM_001195798.1:c.984C= NP_001182727.1:p.Val328=
NM_001195799.1:c.861C= NP_001182728.1:p.Val287=
NM_001195800.1:c.480C= NP_001182729.1:p.Val160=
NM_001195803.1:c.603C= NP_001182732.1:p.Val201=
XM_011528010.1:c.984C= XP_011526312.1:p.Val328=
XM_011528011.1:c.603C= XP_011526313.1:p.Val201=
XR_244074.2:n.1134C=
XM_011528010.2:c.984C= XP_011526312.1:p.Val328=
XR_001753685.2:n.1101C=
XR_001753686.2:n.1101C=
NM_000527.5:c.984C= MANE Select NP_000518.1:p.Val328=
NM_001195798.2:c.984C= NP_001182727.1:p.Val328=
NM_001195799.2:c.861C= NP_001182728.1:p.Val287=
NM_001195800.2:c.480C= NP_001182729.1:p.Val160=
NM_001195803.2:c.603C= NP_001182732.1:p.Val201=