Canonical Allele Identifier: CA2322774413
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11118312_11118314delinsCAG , CM000681.2:g.11118312_11118314delinsCAG GRCh38
NC_000019.9:g.11228988_11228990delinsCAG , CM000681.1:g.11228988_11228990delinsCAG GRCh37
NC_000019.8:g.11089988_11089990delinsCAG NCBI36
NG_009060.1:g.33932_33934delinsCAG , LRG_274:g.33932_33934delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2103+1314_2103+1316delinsCAG ENSP00000252444.6:n.2103+1314_2103+1316delinsCAG
ENST00000559340.2:c.1706-1780_1706-1778delinsCAG ENSP00000453696.2:n.1706-1780_1706-1778delinsCAG
ENST00000560467.2:c.1725+1314_1725+1316delinsCAG ENSP00000453513.2:n.1725+1314_1725+1316delinsCAG
ENST00000558518.6:c.1845+1314_1845+1316delinsCAG MANE Select ENSP00000454071.1:n.1845+1314_1845+1316delinsCAG
ENST00000252444.9:c.2099+1314_2099+1316delinsCAG
ENST00000455727.6:c.1341+1314_1341+1316delinsCAG ENSP00000397829.2:n.1341+1314_1341+1316delinsCAG
ENST00000535915.5:c.1722+1314_1722+1316delinsCAG ENSP00000440520.1:n.1722+1314_1722+1316delinsCAG
ENST00000545707.5:c.1464+1314_1464+1316delinsCAG ENSP00000437639.1:n.1464+1314_1464+1316delinsCAG
ENST00000557933.5:c.1845+1314_1845+1316delinsCAG ENSP00000453557.1:n.1845+1314_1845+1316delinsCAG
ENST00000558013.5:c.1845+1314_1845+1316delinsCAG ENSP00000453346.1:n.1845+1314_1845+1316delinsCAG
ENST00000558518.5:c.1845+1314_1845+1316delinsCAG ENSP00000454071.1:n.1845+1314_1845+1316delinsCAG
ENST00000559340.1:c.427-1780_427-1778delinsCAG
NM_000527.4:c.1845+1314_1845+1316delinsCAG , LRG_274t1:c.1845+1314_1845+1316delinsCAG NP_000518.1:n.1845+1314_1845+1316delinsCAG
NM_001195798.1:c.1845+1314_1845+1316delinsCAG NP_001182727.1:n.1845+1314_1845+1316delinsCAG
NM_001195799.1:c.1722+1314_1722+1316delinsCAG NP_001182728.1:n.1722+1314_1722+1316delinsCAG
NM_001195800.1:c.1341+1314_1341+1316delinsCAG NP_001182729.1:n.1341+1314_1341+1316delinsCAG
NM_001195803.1:c.1464+1314_1464+1316delinsCAG NP_001182732.1:n.1464+1314_1464+1316delinsCAG
XM_011528010.1:c.1845+1314_1845+1316delinsCAG XP_011526312.1:n.1845+1314_1845+1316delinsCAG
XM_011528011.1:c.1464+1314_1464+1316delinsCAG XP_011526313.1:n.1464+1314_1464+1316delinsCAG
XR_244074.2:n.1856-1780_1856-1778delinsCAG
XM_011528010.2:c.1845+1314_1845+1316delinsCAG XP_011526312.1:n.1845+1314_1845+1316delinsCAG
XR_001753685.2:n.1962+1314_1962+1316delinsCAG
XR_001753686.2:n.1823-1780_1823-1778delinsCAG
NM_000527.5:c.1845+1314_1845+1316delinsCAG MANE Select NP_000518.1:n.1845+1314_1845+1316delinsCAG
NM_001195798.2:c.1845+1314_1845+1316delinsCAG NP_001182727.1:n.1845+1314_1845+1316delinsCAG
NM_001195799.2:c.1722+1314_1722+1316delinsCAG NP_001182728.1:n.1722+1314_1722+1316delinsCAG
NM_001195800.2:c.1341+1314_1341+1316delinsCAG NP_001182729.1:n.1341+1314_1341+1316delinsCAG
NM_001195803.2:c.1464+1314_1464+1316delinsCAG NP_001182732.1:n.1464+1314_1464+1316delinsCAG