Canonical Allele Identifier: CA2322768144
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11106572C= , CM000681.2:g.11106572C= GRCh38
NC_000019.9:g.11217248C= , CM000681.1:g.11217248C= GRCh37
NC_000019.8:g.11078248C= NCBI36
NG_009060.1:g.22192C= , LRG_274:g.22192C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.960C= ENSP00000252444.6:p.Ala320=
ENST00000559340.2:c.702C= ENSP00000453696.2:p.Ala234=
ENST00000560467.2:c.702C= ENSP00000453513.2:p.Ala234=
ENST00000558518.6:c.702C= MANE Select ENSP00000454071.1:p.Ala234=
ENST00000252444.9:c.956C=
ENST00000455727.6:c.314-820C= ENSP00000397829.2:n.314-820C=
ENST00000535915.5:c.579C= ENSP00000440520.1:p.Ala193=
ENST00000545707.5:c.321C= ENSP00000437639.1:p.Ala107=
ENST00000557933.5:c.702C= ENSP00000453557.1:p.Ala234=
ENST00000558013.5:c.702C= ENSP00000453346.1:p.Ala234=
ENST00000558518.5:c.702C= ENSP00000454071.1:p.Ala234=
ENST00000558528.1:n.217C=
ENST00000560467.1:c.302C=
NM_000527.4:c.702C= , LRG_274t1:c.702C= NP_000518.1:p.Ala234=
NM_001195798.1:c.702C= NP_001182727.1:p.Ala234=
NM_001195799.1:c.579C= NP_001182728.1:p.Ala193=
NM_001195800.1:c.314-820C= NP_001182729.1:n.314-820C=
NM_001195803.1:c.321C= NP_001182732.1:p.Ala107=
XM_011528010.1:c.702C= XP_011526312.1:p.Ala234=
XM_011528011.1:c.321C= XP_011526313.1:p.Ala107=
XR_244074.2:n.852C=
XM_011528010.2:c.702C= XP_011526312.1:p.Ala234=
XR_001753685.2:n.819C=
XR_001753686.2:n.819C=
NM_000527.5:c.702C= MANE Select NP_000518.1:p.Ala234=
NM_001195798.2:c.702C= NP_001182727.1:p.Ala234=
NM_001195799.2:c.579C= NP_001182728.1:p.Ala193=
NM_001195800.2:c.314-820C= NP_001182729.1:n.314-820C=
NM_001195803.2:c.321C= NP_001182732.1:p.Ala107=