Canonical Allele Identifier: CA993515778

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11132494G>A , CM000681.2:g.11132494G>A GRCh38
NC_000019.9:g.11243170G>A , CM000681.1:g.11243170G>A GRCh37
NC_000019.8:g.11104170G>A NCBI36
NG_009060.1:g.48114G>A , LRG_274:g.48114G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.*1178G>A (LDLR) ENSP00000252444.6:n.*1178G>A
ENST00000559340.2:c.*1830G>A (LDLR) ENSP00000453696.2:n.*1830G>A
ENST00000560467.2:c.*1178G>A (LDLR) ENSP00000453513.2:n.*1178G>A
ENST00000558518.6:c.*1178G>A (LDLR) MANE Select ENSP00000454071.1:n.*1178G>A
ENST00000252444.9:c.4015G>A (LDLR)
ENST00000560628.1:n.109-601G>A (LDLR)
ENST00000585567.5:c.540-887C>T (SPC24) ENSP00000468818.1:n.540-887C>T
NM_000527.4:c.*1178G>A , LRG_274t1:c.*1178G>A (LDLR) NP_000518.1:n.*1178G>A
NM_001195798.1:c.*1178G>A (LDLR) NP_001182727.1:n.*1178G>A
NM_001195799.1:c.*1178G>A (LDLR) NP_001182728.1:n.*1178G>A
NM_001195800.1:c.*1178G>A (LDLR) NP_001182729.1:n.*1178G>A
NM_001195803.1:c.*1178G>A (LDLR) NP_001182732.1:n.*1178G>A
XM_011528010.1:c.*1178G>A (LDLR) XP_011526312.1:n.*1178G>A
XM_011528011.1:c.*1178G>A (LDLR) XP_011526313.1:n.*1178G>A
XM_011528010.2:c.*1178G>A (LDLR) XP_011526312.1:n.*1178G>A
XR_001753685.2:n.4095G>A (LDLR)
XR_001753686.2:n.3738G>A (LDLR)
NM_000527.5:c.*1178G>A (LDLR) MANE Select NP_000518.1:n.*1178G>A
NM_001195798.2:c.*1178G>A (LDLR) NP_001182727.1:n.*1178G>A
NM_001195799.2:c.*1178G>A (LDLR) NP_001182728.1:n.*1178G>A
NM_001195800.2:c.*1178G>A (LDLR) NP_001182729.1:n.*1178G>A
NM_001195803.2:c.*1178G>A (LDLR) NP_001182732.1:n.*1178G>A