Canonical Allele Identifier: CA2322768666
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107514G= , CM000681.2:g.11107514G= GRCh38
NC_000019.9:g.11218190G= , CM000681.1:g.11218190G= GRCh37
NC_000019.8:g.11079190G= NCBI36
NG_009060.1:g.23134G= , LRG_274:g.23134G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1198G= ENSP00000252444.6:p.Gly400=
ENST00000559340.2:c.940G= ENSP00000453696.2:p.Gly314=
ENST00000560467.2:c.940G= ENSP00000453513.2:p.Asp314=
ENST00000558518.6:c.940G= MANE Select ENSP00000454071.1:p.Gly314=
ENST00000252444.9:c.1194G=
ENST00000455727.6:c.436G= ENSP00000397829.2:p.Gly146=
ENST00000535915.5:c.817G= ENSP00000440520.1:p.Gly273=
ENST00000545707.5:c.559G= ENSP00000437639.1:p.Gly187=
ENST00000557933.5:c.940G= ENSP00000453557.1:p.Gly314=
ENST00000558013.5:c.940G= ENSP00000453346.1:p.Gly314=
ENST00000558518.5:c.940G= ENSP00000454071.1:p.Gly314=
ENST00000558528.1:n.455G=
ENST00000560467.1:c.540G=
NM_000527.4:c.940G= , LRG_274t1:c.940G= NP_000518.1:p.Gly314=
NM_001195798.1:c.940G= NP_001182727.1:p.Gly314=
NM_001195799.1:c.817G= NP_001182728.1:p.Gly273=
NM_001195800.1:c.436G= NP_001182729.1:p.Gly146=
NM_001195803.1:c.559G= NP_001182732.1:p.Gly187=
XM_011528010.1:c.940G= XP_011526312.1:p.Gly314=
XM_011528011.1:c.559G= XP_011526313.1:p.Gly187=
XR_244074.2:n.1090G=
XM_011528010.2:c.940G= XP_011526312.1:p.Gly314=
XR_001753685.2:n.1057G=
XR_001753686.2:n.1057G=
NM_000527.5:c.940G= MANE Select NP_000518.1:p.Gly314=
NM_001195798.2:c.940G= NP_001182727.1:p.Gly314=
NM_001195799.2:c.817G= NP_001182728.1:p.Gly273=
NM_001195800.2:c.436G= NP_001182729.1:p.Gly146=
NM_001195803.2:c.559G= NP_001182732.1:p.Gly187=