Canonical Allele Identifier: CA2322773655
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116880A= , CM000681.2:g.11116880A= GRCh38
NC_000019.9:g.11227556A= , CM000681.1:g.11227556A= GRCh37
NC_000019.8:g.11088556A= NCBI36
NG_009060.1:g.32500A= , LRG_274:g.32500A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1985A= ENSP00000252444.6:p.Tyr662=
ENST00000559340.2:c.1705+668A= ENSP00000453696.2:n.1705+668A=
ENST00000560467.2:c.1607A= ENSP00000453513.2:p.Tyr536=
ENST00000558518.6:c.1727A= MANE Select ENSP00000454071.1:p.Tyr576=
ENST00000252444.9:c.1981A=
ENST00000455727.6:c.1223A= ENSP00000397829.2:p.Tyr408=
ENST00000535915.5:c.1604A= ENSP00000440520.1:p.Tyr535=
ENST00000545707.5:c.1346A= ENSP00000437639.1:p.Tyr449=
ENST00000557933.5:c.1727A= ENSP00000453557.1:p.Tyr576=
ENST00000558013.5:c.1727A= ENSP00000453346.1:p.Tyr576=
ENST00000558518.5:c.1727A= ENSP00000454071.1:p.Tyr576=
ENST00000559340.1:c.426+668A=
NM_000527.4:c.1727A= , LRG_274t1:c.1727A= NP_000518.1:p.Tyr576=
NM_001195798.1:c.1727A= NP_001182727.1:p.Tyr576=
NM_001195799.1:c.1604A= NP_001182728.1:p.Tyr535=
NM_001195800.1:c.1223A= NP_001182729.1:p.Tyr408=
NM_001195803.1:c.1346A= NP_001182732.1:p.Tyr449=
XM_011528010.1:c.1727A= XP_011526312.1:p.Tyr576=
XM_011528011.1:c.1346A= XP_011526313.1:p.Tyr449=
XR_244074.2:n.1855+668A=
XM_011528010.2:c.1727A= XP_011526312.1:p.Tyr576=
XR_001753685.2:n.1844A=
XR_001753686.2:n.1822+668A=
NM_000527.5:c.1727A= MANE Select NP_000518.1:p.Tyr576=
NM_001195798.2:c.1727A= NP_001182727.1:p.Tyr576=
NM_001195799.2:c.1604A= NP_001182728.1:p.Tyr535=
NM_001195800.2:c.1223A= NP_001182729.1:p.Tyr408=
NM_001195803.2:c.1346A= NP_001182732.1:p.Tyr449=