Canonical Allele Identifier: CA2322770609
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11111372T= , CM000681.2:g.11111372T= GRCh38
NC_000019.9:g.11222048T= , CM000681.1:g.11222048T= GRCh37
NC_000019.8:g.11083048T= NCBI36
NG_009060.1:g.26992T= , LRG_274:g.26992T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1319-142T= ENSP00000252444.6:n.1319-142T=
ENST00000559340.2:c.1061-142T= ENSP00000453696.2:n.1061-142T=
ENST00000560467.2:c.941-142T= ENSP00000453513.2:n.941-142T=
ENST00000558518.6:c.1061-142T= MANE Select ENSP00000454071.1:n.1061-142T=
ENST00000252444.9:c.1315-142T=
ENST00000455727.6:c.557-142T= ENSP00000397829.2:n.557-142T=
ENST00000535915.5:c.938-142T= ENSP00000440520.1:n.938-142T=
ENST00000545707.5:c.680-142T= ENSP00000437639.1:n.680-142T=
ENST00000557933.5:c.1061-142T= ENSP00000453557.1:n.1061-142T=
ENST00000558013.5:c.1061-142T= ENSP00000453346.1:n.1061-142T=
ENST00000558518.5:c.1061-142T= ENSP00000454071.1:n.1061-142T=
ENST00000560173.1:n.60-142T=
ENST00000560467.1:c.541-142T=
NM_000527.4:c.1061-142T= , LRG_274t1:c.1061-142T= NP_000518.1:n.1061-142T=
NM_001195798.1:c.1061-142T= NP_001182727.1:n.1061-142T=
NM_001195799.1:c.938-142T= NP_001182728.1:n.938-142T=
NM_001195800.1:c.557-142T= NP_001182729.1:n.557-142T=
NM_001195803.1:c.680-142T= NP_001182732.1:n.680-142T=
XM_011528010.1:c.1061-142T= XP_011526312.1:n.1061-142T=
XM_011528011.1:c.680-142T= XP_011526313.1:n.680-142T=
XR_244074.2:n.1211-142T=
XM_011528010.2:c.1061-142T= XP_011526312.1:n.1061-142T=
XR_001753685.2:n.1178-142T=
XR_001753686.2:n.1178-142T=
NM_000527.5:c.1061-142T= MANE Select NP_000518.1:n.1061-142T=
NM_001195798.2:c.1061-142T= NP_001182727.1:n.1061-142T=
NM_001195799.2:c.938-142T= NP_001182728.1:n.938-142T=
NM_001195800.2:c.557-142T= NP_001182729.1:n.557-142T=
NM_001195803.2:c.680-142T= NP_001182732.1:n.680-142T=