Canonical Allele Identifier: CA2322771849
Gene: LDLR HGNC NCBI
MIR6886 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113506G= , CM000681.2:g.11113506G= GRCh38
NC_000019.9:g.11224182G= , CM000681.1:g.11224182G= GRCh37
NC_000019.8:g.11085182G= NCBI36
NG_009060.1:g.29126G= , LRG_274:g.29126G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1617-29G= (LDLR) ENSP00000252444.6:n.1617-29G=
ENST00000559340.2:c.1359-29G= (LDLR) ENSP00000453696.2:n.1359-29G=
ENST00000560467.2:c.1239-29G= (LDLR) ENSP00000453513.2:n.1239-29G=
ENST00000558518.6:c.1359-29G= (LDLR) MANE Select ENSP00000454071.1:n.1359-29G=
ENST00000252444.9:c.1613-29G= (LDLR)
ENST00000455727.6:c.855-29G= (LDLR) ENSP00000397829.2:n.855-29G=
ENST00000535915.5:c.1236-29G= (LDLR) ENSP00000440520.1:n.1236-29G=
ENST00000545707.5:c.978-29G= (LDLR) ENSP00000437639.1:n.978-29G=
ENST00000557933.5:c.1359-29G= (LDLR) ENSP00000453557.1:n.1359-29G=
ENST00000558013.5:c.1359-29G= (LDLR) ENSP00000453346.1:n.1359-29G=
ENST00000558518.5:c.1359-29G= (LDLR) ENSP00000454071.1:n.1359-29G=
ENST00000559340.1:c.80-29G= (LDLR)
ENST00000560467.1:c.839-29G= (LDLR)
NM_000527.4:c.1359-29G= , LRG_274t1:c.1359-29G= (LDLR) NP_000518.1:n.1359-29G=
NM_001195798.1:c.1359-29G= (LDLR) NP_001182727.1:n.1359-29G=
NM_001195799.1:c.1236-29G= (LDLR) NP_001182728.1:n.1236-29G=
NM_001195800.1:c.855-29G= (LDLR) NP_001182729.1:n.855-29G=
NM_001195803.1:c.978-29G= (LDLR) NP_001182732.1:n.978-29G=
NR_106946.1:n.33G= (MIR6886)
XM_011528010.1:c.1359-29G= (LDLR) XP_011526312.1:n.1359-29G=
XM_011528011.1:c.978-29G= (LDLR) XP_011526313.1:n.978-29G=
XR_244074.2:n.1509-29G= (LDLR)
XM_011528010.2:c.1359-29G= (LDLR) XP_011526312.1:n.1359-29G=
XR_001753685.2:n.1476-29G= (LDLR)
XR_001753686.2:n.1476-29G= (LDLR)
NM_000527.5:c.1359-29G= (LDLR) MANE Select NP_000518.1:n.1359-29G=
NM_001195798.2:c.1359-29G= (LDLR) NP_001182727.1:n.1359-29G=
NM_001195799.2:c.1236-29G= (LDLR) NP_001182728.1:n.1236-29G=
NM_001195800.2:c.855-29G= (LDLR) NP_001182729.1:n.855-29G=
NM_001195803.2:c.978-29G= (LDLR) NP_001182732.1:n.978-29G=