Canonical Allele Identifier: CA2322769224
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs2077332626

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11108543_11108546del , CM000681.2:g.11108543_11108546del GRCh38
NC_000019.9:g.11219219_11219222del , CM000681.1:g.11219219_11219222del GRCh37
NC_000019.8:g.11080219_11080222del NCBI36
NG_009060.1:g.24163_24166del , LRG_274:g.24163_24166del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1198+1029_1198+1032del ENSP00000252444.6:n.1198+1029_1198+1032del
ENST00000559340.2:c.940+1029_940+1032del ENSP00000453696.2:n.940+1029_940+1032del
ENST00000560467.2:c.940+1029_940+1032del ENSP00000453513.2:n.940+1029_940+1032del
ENST00000558518.6:c.940+1029_940+1032del MANE Select ENSP00000454071.1:n.940+1029_940+1032del
ENST00000252444.9:c.1194+1029_1194+1032del
ENST00000455727.6:c.436+1029_436+1032del ENSP00000397829.2:n.436+1029_436+1032del
ENST00000535915.5:c.817+1029_817+1032del ENSP00000440520.1:n.817+1029_817+1032del
ENST00000545707.5:c.559+1029_559+1032del ENSP00000437639.1:n.559+1029_559+1032del
ENST00000557933.5:c.940+1029_940+1032del ENSP00000453557.1:n.940+1029_940+1032del
ENST00000558013.5:c.940+1029_940+1032del ENSP00000453346.1:n.940+1029_940+1032del
ENST00000558518.5:c.940+1029_940+1032del ENSP00000454071.1:n.940+1029_940+1032del
ENST00000560467.1:c.540+1029_540+1032del
NM_000527.4:c.940+1029_940+1032del , LRG_274t1:c.940+1029_940+1032del NP_000518.1:n.940+1029_940+1032del
NM_001195798.1:c.940+1029_940+1032del NP_001182727.1:n.940+1029_940+1032del
NM_001195799.1:c.817+1029_817+1032del NP_001182728.1:n.817+1029_817+1032del
NM_001195800.1:c.436+1029_436+1032del NP_001182729.1:n.436+1029_436+1032del
NM_001195803.1:c.559+1029_559+1032del NP_001182732.1:n.559+1029_559+1032del
XM_011528010.1:c.940+1029_940+1032del XP_011526312.1:n.940+1029_940+1032del
XM_011528011.1:c.559+1029_559+1032del XP_011526313.1:n.559+1029_559+1032del
XR_244074.2:n.1090+1029_1090+1032del
XM_011528010.2:c.940+1029_940+1032del XP_011526312.1:n.940+1029_940+1032del
XR_001753685.2:n.1057+1029_1057+1032del
XR_001753686.2:n.1057+1029_1057+1032del
NM_000527.5:c.940+1029_940+1032del MANE Select NP_000518.1:n.940+1029_940+1032del
NM_001195798.2:c.940+1029_940+1032del NP_001182727.1:n.940+1029_940+1032del
NM_001195799.2:c.817+1029_817+1032del NP_001182728.1:n.817+1029_817+1032del
NM_001195800.2:c.436+1029_436+1032del NP_001182729.1:n.436+1029_436+1032del
NM_001195803.2:c.559+1029_559+1032del NP_001182732.1:n.559+1029_559+1032del