Canonical Allele Identifier: CA2322770417
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11110982G= , CM000681.2:g.11110982G= GRCh38
NC_000019.9:g.11221658G= , CM000681.1:g.11221658G= GRCh37
NC_000019.8:g.11082658G= NCBI36
NG_009060.1:g.26602G= , LRG_274:g.26602G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1318+211G= ENSP00000252444.6:n.1318+211G=
ENST00000559340.2:c.1060+211G= ENSP00000453696.2:n.1060+211G=
ENST00000560467.2:c.941-532G= ENSP00000453513.2:n.941-532G=
ENST00000558518.6:c.1060+211G= MANE Select ENSP00000454071.1:n.1060+211G=
ENST00000252444.9:c.1314+211G=
ENST00000455727.6:c.556+211G= ENSP00000397829.2:n.556+211G=
ENST00000535915.5:c.937+211G= ENSP00000440520.1:n.937+211G=
ENST00000545707.5:c.679+211G= ENSP00000437639.1:n.679+211G=
ENST00000557933.5:c.1060+211G= ENSP00000453557.1:n.1060+211G=
ENST00000558013.5:c.1060+211G= ENSP00000453346.1:n.1060+211G=
ENST00000558518.5:c.1060+211G= ENSP00000454071.1:n.1060+211G=
ENST00000560173.1:n.59+211G=
ENST00000560467.1:c.541-532G=
NM_000527.4:c.1060+211G= , LRG_274t1:c.1060+211G= NP_000518.1:n.1060+211G=
NM_001195798.1:c.1060+211G= NP_001182727.1:n.1060+211G=
NM_001195799.1:c.937+211G= NP_001182728.1:n.937+211G=
NM_001195800.1:c.556+211G= NP_001182729.1:n.556+211G=
NM_001195803.1:c.679+211G= NP_001182732.1:n.679+211G=
XM_011528010.1:c.1060+211G= XP_011526312.1:n.1060+211G=
XM_011528011.1:c.679+211G= XP_011526313.1:n.679+211G=
XR_244074.2:n.1210+211G=
XM_011528010.2:c.1060+211G= XP_011526312.1:n.1060+211G=
XR_001753685.2:n.1177+211G=
XR_001753686.2:n.1177+211G=
NM_000527.5:c.1060+211G= MANE Select NP_000518.1:n.1060+211G=
NM_001195798.2:c.1060+211G= NP_001182727.1:n.1060+211G=
NM_001195799.2:c.937+211G= NP_001182728.1:n.937+211G=
NM_001195800.2:c.556+211G= NP_001182729.1:n.556+211G=
NM_001195803.2:c.679+211G= NP_001182732.1:n.679+211G=