Canonical Allele Identifier: CA2322772032
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113727C= , CM000681.2:g.11113727C= GRCh38
NC_000019.9:g.11224403C= , CM000681.1:g.11224403C= GRCh37
NC_000019.8:g.11085403C= NCBI36
NG_009060.1:g.29347C= , LRG_274:g.29347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1809C= ENSP00000252444.6:p.Ser603=
ENST00000559340.2:c.1551C= ENSP00000453696.2:p.Ser517=
ENST00000560467.2:c.1431C= ENSP00000453513.2:p.Ser477=
ENST00000558518.6:c.1551C= MANE Select ENSP00000454071.1:p.Ser517=
ENST00000252444.9:c.1805C=
ENST00000455727.6:c.1047C= ENSP00000397829.2:p.Ser349=
ENST00000535915.5:c.1428C= ENSP00000440520.1:p.Ser476=
ENST00000545707.5:c.1170C= ENSP00000437639.1:p.Ser390=
ENST00000557933.5:c.1551C= ENSP00000453557.1:p.Ser517=
ENST00000558013.5:c.1551C= ENSP00000453346.1:p.Ser517=
ENST00000558518.5:c.1551C= ENSP00000454071.1:p.Ser517=
ENST00000559340.1:c.272C=
NM_000527.4:c.1551C= , LRG_274t1:c.1551C= NP_000518.1:p.Ser517=
NM_001195798.1:c.1551C= NP_001182727.1:p.Ser517=
NM_001195799.1:c.1428C= NP_001182728.1:p.Ser476=
NM_001195800.1:c.1047C= NP_001182729.1:p.Ser349=
NM_001195803.1:c.1170C= NP_001182732.1:p.Ser390=
XM_011528010.1:c.1551C= XP_011526312.1:p.Ser517=
XM_011528011.1:c.1170C= XP_011526313.1:p.Ser390=
XR_244074.2:n.1701C=
XM_011528010.2:c.1551C= XP_011526312.1:p.Ser517=
XR_001753685.2:n.1668C=
XR_001753686.2:n.1668C=
NM_000527.5:c.1551C= MANE Select NP_000518.1:p.Ser517=
NM_001195798.2:c.1551C= NP_001182727.1:p.Ser517=
NM_001195799.2:c.1428C= NP_001182728.1:p.Ser476=
NM_001195800.2:c.1047C= NP_001182729.1:p.Ser349=
NM_001195803.2:c.1170C= NP_001182732.1:p.Ser390=