Canonical Allele Identifier: CA2322770273
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110720G= , CM000681.2:g.11110720G= GRCh38
NC_000019.9:g.11221396G= , CM000681.1:g.11221396G= GRCh37
NC_000019.8:g.11082396G= NCBI36
NG_009060.1:g.26340G= , LRG_274:g.26340G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1267G= ENSP00000252444.6:p.Glu423=
ENST00000559340.2:c.1009G= ENSP00000453696.2:p.Glu337=
ENST00000560467.2:c.941-794G= ENSP00000453513.2:n.941-794G=
ENST00000558518.6:c.1009G= MANE Select ENSP00000454071.1:p.Glu337=
ENST00000252444.9:c.1263G=
ENST00000455727.6:c.505G= ENSP00000397829.2:p.Glu169=
ENST00000535915.5:c.886G= ENSP00000440520.1:p.Glu296=
ENST00000545707.5:c.628G= ENSP00000437639.1:p.Glu210=
ENST00000557933.5:c.1009G= ENSP00000453557.1:p.Glu337=
ENST00000558013.5:c.1009G= ENSP00000453346.1:p.Glu337=
ENST00000558518.5:c.1009G= ENSP00000454071.1:p.Glu337=
ENST00000560173.1:n.8G=
ENST00000560467.1:c.541-794G=
NM_000527.4:c.1009G= , LRG_274t1:c.1009G= NP_000518.1:p.Glu337=
NM_001195798.1:c.1009G= NP_001182727.1:p.Glu337=
NM_001195799.1:c.886G= NP_001182728.1:p.Glu296=
NM_001195800.1:c.505G= NP_001182729.1:p.Glu169=
NM_001195803.1:c.628G= NP_001182732.1:p.Glu210=
XM_011528010.1:c.1009G= XP_011526312.1:p.Glu337=
XM_011528011.1:c.628G= XP_011526313.1:p.Glu210=
XR_244074.2:n.1159G=
XM_011528010.2:c.1009G= XP_011526312.1:p.Glu337=
XR_001753685.2:n.1126G=
XR_001753686.2:n.1126G=
NM_000527.5:c.1009G= MANE Select NP_000518.1:p.Glu337=
NM_001195798.2:c.1009G= NP_001182727.1:p.Glu337=
NM_001195799.2:c.886G= NP_001182728.1:p.Glu296=
NM_001195800.2:c.505G= NP_001182729.1:p.Glu169=
NM_001195803.2:c.628G= NP_001182732.1:p.Glu210=