Canonical Allele Identifier: CA631767767
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11117930_11117931insT , CM000681.2:g.11117930_11117931insT GRCh38
NC_000019.9:g.11228606_11228607insT , CM000681.1:g.11228606_11228607insT GRCh37
NC_000019.8:g.11089606_11089607insT NCBI36
NG_009060.1:g.33550_33551insT , LRG_274:g.33550_33551insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2103+932_2103+933insT ENSP00000252444.6:n.2103+932_2103+933insT
ENST00000559340.2:c.1705+1718_1705+1719insT ENSP00000453696.2:n.1705+1718_1705+1719insT
ENST00000560467.2:c.1725+932_1725+933insT ENSP00000453513.2:n.1725+932_1725+933insT
ENST00000558518.6:c.1845+932_1845+933insT MANE Select ENSP00000454071.1:n.1845+932_1845+933insT
ENST00000252444.9:c.2099+932_2099+933insT
ENST00000455727.6:c.1341+932_1341+933insT ENSP00000397829.2:n.1341+932_1341+933insT
ENST00000535915.5:c.1722+932_1722+933insT ENSP00000440520.1:n.1722+932_1722+933insT
ENST00000545707.5:c.1464+932_1464+933insT ENSP00000437639.1:n.1464+932_1464+933insT
ENST00000557933.5:c.1845+932_1845+933insT ENSP00000453557.1:n.1845+932_1845+933insT
ENST00000558013.5:c.1845+932_1845+933insT ENSP00000453346.1:n.1845+932_1845+933insT
ENST00000558518.5:c.1845+932_1845+933insT ENSP00000454071.1:n.1845+932_1845+933insT
ENST00000559340.1:c.426+1718_426+1719insT
NM_000527.4:c.1845+932_1845+933insT , LRG_274t1:c.1845+932_1845+933insT NP_000518.1:n.1845+932_1845+933insT
NM_001195798.1:c.1845+932_1845+933insT NP_001182727.1:n.1845+932_1845+933insT
NM_001195799.1:c.1722+932_1722+933insT NP_001182728.1:n.1722+932_1722+933insT
NM_001195800.1:c.1341+932_1341+933insT NP_001182729.1:n.1341+932_1341+933insT
NM_001195803.1:c.1464+932_1464+933insT NP_001182732.1:n.1464+932_1464+933insT
XM_011528010.1:c.1845+932_1845+933insT XP_011526312.1:n.1845+932_1845+933insT
XM_011528011.1:c.1464+932_1464+933insT XP_011526313.1:n.1464+932_1464+933insT
XR_244074.2:n.1855+1718_1855+1719insT
XM_011528010.2:c.1845+932_1845+933insT XP_011526312.1:n.1845+932_1845+933insT
XR_001753685.2:n.1962+932_1962+933insT
XR_001753686.2:n.1822+1718_1822+1719insT
NM_000527.5:c.1845+932_1845+933insT MANE Select NP_000518.1:n.1845+932_1845+933insT
NM_001195798.2:c.1845+932_1845+933insT NP_001182727.1:n.1845+932_1845+933insT
NM_001195799.2:c.1722+932_1722+933insT NP_001182728.1:n.1722+932_1722+933insT
NM_001195800.2:c.1341+932_1341+933insT NP_001182729.1:n.1341+932_1341+933insT
NM_001195803.2:c.1464+932_1464+933insT NP_001182732.1:n.1464+932_1464+933insT