Canonical Allele Identifier: CA030025
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs757086563

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11107460_11107461insA , CM000681.2:g.11107460_11107461insA GRCh38
NC_000019.9:g.11218136_11218137insA , CM000681.1:g.11218136_11218137insA GRCh37
NC_000019.8:g.11079136_11079137insA NCBI36
NG_009060.1:g.23080_23081insA , LRG_274:g.23080_23081insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1144_1145insA ENSP00000252444.6:p.Cys382Ter
ENST00000559340.2:c.886_887insA ENSP00000453696.2:p.Cys296Ter
ENST00000560467.2:c.886_887insA ENSP00000453513.2:p.Cys296Ter
ENST00000558518.6:c.886_887insA MANE Select ENSP00000454071.1:p.Cys296Ter
ENST00000252444.9:c.1140_1141insA
ENST00000455727.6:c.382_383insA ENSP00000397829.2:p.Cys128Ter
ENST00000535915.5:c.763_764insA ENSP00000440520.1:p.Cys255Ter
ENST00000545707.5:c.505_506insA ENSP00000437639.1:p.Cys169Ter
ENST00000557933.5:c.886_887insA ENSP00000453557.1:p.Cys296Ter
ENST00000558013.5:c.886_887insA ENSP00000453346.1:p.Cys296Ter
ENST00000558518.5:c.886_887insA ENSP00000454071.1:p.Cys296Ter
ENST00000558528.1:n.401_402insA
ENST00000560467.1:c.486_487insA
NM_000527.4:c.886_887insA , LRG_274t1:c.886_887insA NP_000518.1:p.Cys296Ter
NM_001195798.1:c.886_887insA NP_001182727.1:p.Cys296Ter
NM_001195799.1:c.763_764insA NP_001182728.1:p.Cys255Ter
NM_001195800.1:c.382_383insA NP_001182729.1:p.Cys128Ter
NM_001195803.1:c.505_506insA NP_001182732.1:p.Cys169Ter
XM_011528010.1:c.886_887insA XP_011526312.1:p.Cys296Ter
XM_011528011.1:c.505_506insA XP_011526313.1:p.Cys169Ter
XR_244074.2:n.1036_1037insA
XM_011528010.2:c.886_887insA XP_011526312.1:p.Cys296Ter
XR_001753685.2:n.1003_1004insA
XR_001753686.2:n.1003_1004insA
NM_000527.5:c.886_887insA MANE Select NP_000518.1:p.Cys296Ter
NM_001195798.2:c.886_887insA NP_001182727.1:p.Cys296Ter
NM_001195799.2:c.763_764insA NP_001182728.1:p.Cys255Ter
NM_001195800.2:c.382_383insA NP_001182729.1:p.Cys128Ter
NM_001195803.2:c.505_506insA NP_001182732.1:p.Cys169Ter