Canonical Allele Identifier: CA10585419
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251804
ClinVar RCV Id: RCV000237521
dbSNP Id: rs879254875

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113452_11113457del , CM000681.2:g.11113452_11113457del GRCh38
NC_000019.9:g.11224128_11224133del , CM000681.1:g.11224128_11224133del GRCh37
NC_000019.8:g.11085128_11085133del NCBI36
NG_009060.1:g.29072_29077del , LRG_274:g.29072_29077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1616+3_1616+8del ENSP00000252444.6:n.1616+3_1616+8del
ENST00000559340.2:c.1358+3_1358+8del ENSP00000453696.2:n.1358+3_1358+8del
ENST00000560467.2:c.1238+3_1238+8del ENSP00000453513.2:n.1238+3_1238+8del
ENST00000558518.6:c.1358+3_1358+8del MANE Select ENSP00000454071.1:n.1358+3_1358+8del
ENST00000252444.9:c.1612+3_1612+8del
ENST00000455727.6:c.854+3_854+8del ENSP00000397829.2:n.854+3_854+8del
ENST00000535915.5:c.1235+3_1235+8del ENSP00000440520.1:n.1235+3_1235+8del
ENST00000545707.5:c.977+3_977+8del ENSP00000437639.1:n.977+3_977+8del
ENST00000557933.5:c.1358+3_1358+8del ENSP00000453557.1:n.1358+3_1358+8del
ENST00000558013.5:c.1358+3_1358+8del ENSP00000453346.1:n.1358+3_1358+8del
ENST00000558518.5:c.1358+3_1358+8del ENSP00000454071.1:n.1358+3_1358+8del
ENST00000559340.1:c.79+3_79+8del
ENST00000560173.1:n.360_365del
ENST00000560467.1:c.838+3_838+8del
NM_000527.4:c.1358+3_1358+8del , LRG_274t1:c.1358+3_1358+8del NP_000518.1:n.1358+3_1358+8del
NM_001195798.1:c.1358+3_1358+8del NP_001182727.1:n.1358+3_1358+8del
NM_001195799.1:c.1235+3_1235+8del NP_001182728.1:n.1235+3_1235+8del
NM_001195800.1:c.854+3_854+8del NP_001182729.1:n.854+3_854+8del
NM_001195803.1:c.977+3_977+8del NP_001182732.1:n.977+3_977+8del
XM_011528010.1:c.1358+3_1358+8del XP_011526312.1:n.1358+3_1358+8del
XM_011528011.1:c.977+3_977+8del XP_011526313.1:n.977+3_977+8del
XR_244074.2:n.1508+3_1508+8del
XM_011528010.2:c.1358+3_1358+8del XP_011526312.1:n.1358+3_1358+8del
XR_001753685.2:n.1475+3_1475+8del
XR_001753686.2:n.1475+3_1475+8del
NM_000527.5:c.1358+3_1358+8del MANE Select NP_000518.1:n.1358+3_1358+8del
NM_001195798.2:c.1358+3_1358+8del NP_001182727.1:n.1358+3_1358+8del
NM_001195799.2:c.1235+3_1235+8del NP_001182728.1:n.1235+3_1235+8del
NM_001195800.2:c.854+3_854+8del NP_001182729.1:n.854+3_854+8del
NM_001195803.2:c.977+3_977+8del NP_001182732.1:n.977+3_977+8del