Canonical Allele Identifier: CA2322773834
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11117136_11117138delinsTTC , CM000681.2:g.11117136_11117138delinsTTC GRCh38
NC_000019.9:g.11227812_11227814delinsTTC , CM000681.1:g.11227812_11227814delinsTTC GRCh37
NC_000019.8:g.11088812_11088814delinsTTC NCBI36
NG_009060.1:g.32756_32758delinsTTC , LRG_274:g.32756_32758delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2103+138_2103+140delinsTTC ENSP00000252444.6:n.2103+138_2103+140delinsTTC
ENST00000559340.2:c.1705+924_1705+926delinsTTC ENSP00000453696.2:n.1705+924_1705+926delinsTTC
ENST00000560467.2:c.1725+138_1725+140delinsTTC ENSP00000453513.2:n.1725+138_1725+140delinsTTC
ENST00000558518.6:c.1845+138_1845+140delinsTTC MANE Select ENSP00000454071.1:n.1845+138_1845+140delinsTTC
ENST00000252444.9:c.2099+138_2099+140delinsTTC
ENST00000455727.6:c.1341+138_1341+140delinsTTC ENSP00000397829.2:n.1341+138_1341+140delinsTTC
ENST00000535915.5:c.1722+138_1722+140delinsTTC ENSP00000440520.1:n.1722+138_1722+140delinsTTC
ENST00000545707.5:c.1464+138_1464+140delinsTTC ENSP00000437639.1:n.1464+138_1464+140delinsTTC
ENST00000557933.5:c.1845+138_1845+140delinsTTC ENSP00000453557.1:n.1845+138_1845+140delinsTTC
ENST00000558013.5:c.1845+138_1845+140delinsTTC ENSP00000453346.1:n.1845+138_1845+140delinsTTC
ENST00000558518.5:c.1845+138_1845+140delinsTTC ENSP00000454071.1:n.1845+138_1845+140delinsTTC
ENST00000559340.1:c.426+924_426+926delinsTTC
NM_000527.4:c.1845+138_1845+140delinsTTC , LRG_274t1:c.1845+138_1845+140delinsTTC NP_000518.1:n.1845+138_1845+140delinsTTC
NM_001195798.1:c.1845+138_1845+140delinsTTC NP_001182727.1:n.1845+138_1845+140delinsTTC
NM_001195799.1:c.1722+138_1722+140delinsTTC NP_001182728.1:n.1722+138_1722+140delinsTTC
NM_001195800.1:c.1341+138_1341+140delinsTTC NP_001182729.1:n.1341+138_1341+140delinsTTC
NM_001195803.1:c.1464+138_1464+140delinsTTC NP_001182732.1:n.1464+138_1464+140delinsTTC
XM_011528010.1:c.1845+138_1845+140delinsTTC XP_011526312.1:n.1845+138_1845+140delinsTTC
XM_011528011.1:c.1464+138_1464+140delinsTTC XP_011526313.1:n.1464+138_1464+140delinsTTC
XR_244074.2:n.1855+924_1855+926delinsTTC
XM_011528010.2:c.1845+138_1845+140delinsTTC XP_011526312.1:n.1845+138_1845+140delinsTTC
XR_001753685.2:n.1962+138_1962+140delinsTTC
XR_001753686.2:n.1822+924_1822+926delinsTTC
NM_000527.5:c.1845+138_1845+140delinsTTC MANE Select NP_000518.1:n.1845+138_1845+140delinsTTC
NM_001195798.2:c.1845+138_1845+140delinsTTC NP_001182727.1:n.1845+138_1845+140delinsTTC
NM_001195799.2:c.1722+138_1722+140delinsTTC NP_001182728.1:n.1722+138_1722+140delinsTTC
NM_001195800.2:c.1341+138_1341+140delinsTTC NP_001182729.1:n.1341+138_1341+140delinsTTC
NM_001195803.2:c.1464+138_1464+140delinsTTC NP_001182732.1:n.1464+138_1464+140delinsTTC