Canonical Allele Identifier: CA2322775567
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120415A= , CM000681.2:g.11120415A= GRCh38
NC_000019.9:g.11231091A= , CM000681.1:g.11231091A= GRCh37
NC_000019.8:g.11092091A= NCBI36
NG_009060.1:g.36035A= , LRG_274:g.36035A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2291A= ENSP00000252444.6:p.Gln764=
ENST00000559340.2:c.*102A= ENSP00000453696.2:n.*102A=
ENST00000560467.2:c.1913A= ENSP00000453513.2:p.Gln638=
ENST00000558518.6:c.2033A= MANE Select ENSP00000454071.1:p.Gln678=
ENST00000252444.9:c.2287A=
ENST00000455727.6:c.1529A= ENSP00000397829.2:p.Gln510=
ENST00000535915.5:c.1910A= ENSP00000440520.1:p.Gln637=
ENST00000545707.5:c.1606+182A= ENSP00000437639.1:n.1606+182A=
ENST00000557933.5:c.2033A= ENSP00000453557.1:p.Gln678=
ENST00000558013.5:c.2033A= ENSP00000453346.1:p.Gln678=
ENST00000558518.5:c.2033A= ENSP00000454071.1:p.Gln678=
NM_000527.4:c.2033A= , LRG_274t1:c.2033A= NP_000518.1:p.Gln678=
NM_001195798.1:c.2033A= NP_001182727.1:p.Gln678=
NM_001195799.1:c.1910A= NP_001182728.1:p.Gln637=
NM_001195800.1:c.1529A= NP_001182729.1:p.Gln510=
NM_001195803.1:c.1606+182A= NP_001182732.1:n.1606+182A=
XM_011528010.1:c.2033A= XP_011526312.1:p.Gln678=
XM_011528011.1:c.1652A= XP_011526313.1:p.Gln551=
XR_244074.2:n.2043A=
XM_011528010.2:c.2033A= XP_011526312.1:p.Gln678=
XR_001753685.2:n.2150A=
XR_001753686.2:n.2010A=
NM_000527.5:c.2033A= MANE Select NP_000518.1:p.Gln678=
NM_001195798.2:c.2033A= NP_001182727.1:p.Gln678=
NM_001195799.2:c.1910A= NP_001182728.1:p.Gln637=
NM_001195800.2:c.1529A= NP_001182729.1:p.Gln510=
NM_001195803.2:c.1606+182A= NP_001182732.1:n.1606+182A=