Canonical Allele Identifier: CA2322766062
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11102777C= , CM000681.2:g.11102777C= GRCh38
NC_000019.9:g.11213453C= , CM000681.1:g.11213453C= GRCh37
NC_000019.8:g.11074453C= NCBI36
NG_009060.1:g.18397C= , LRG_274:g.18397C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.562C= ENSP00000252444.6:p.Gln188=
ENST00000559340.2:c.304C= ENSP00000453696.2:p.Gln102=
ENST00000560467.2:c.304C= ENSP00000453513.2:p.Gln102=
ENST00000558518.6:c.304C= MANE Select ENSP00000454071.1:p.Gln102=
ENST00000252444.9:c.558C=
ENST00000455727.6:c.304C= ENSP00000397829.2:p.Gln102=
ENST00000535915.5:c.190+2432C= ENSP00000440520.1:n.190+2432C=
ENST00000545707.5:c.304C= ENSP00000437639.1:p.Gln102=
ENST00000557933.5:c.304C= ENSP00000453557.1:p.Gln102=
ENST00000557958.1:n.390C=
ENST00000558013.5:c.304C= ENSP00000453346.1:p.Gln102=
ENST00000558518.5:c.304C= ENSP00000454071.1:p.Gln102=
NM_000527.4:c.304C= , LRG_274t1:c.304C= NP_000518.1:p.Gln102=
NM_001195798.1:c.304C= NP_001182727.1:p.Gln102=
NM_001195799.1:c.190+2432C= NP_001182728.1:n.190+2432C=
NM_001195800.1:c.304C= NP_001182729.1:p.Gln102=
NM_001195803.1:c.304C= NP_001182732.1:p.Gln102=
XM_011528010.1:c.304C= XP_011526312.1:p.Gln102=
XM_011528011.1:c.304C= XP_011526313.1:p.Gln102=
XR_244074.2:n.454C=
XM_011528010.2:c.304C= XP_011526312.1:p.Gln102=
XR_001753685.2:n.421C=
XR_001753686.2:n.421C=
NM_000527.5:c.304C= MANE Select NP_000518.1:p.Gln102=
NM_001195798.2:c.304C= NP_001182727.1:p.Gln102=
NM_001195799.2:c.190+2432C= NP_001182728.1:n.190+2432C=
NM_001195800.2:c.304C= NP_001182729.1:p.Gln102=
NM_001195803.2:c.304C= NP_001182732.1:p.Gln102=