Canonical Allele Identifier: CA404083474
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 430772
ClinVar RCV Id: RCV000495909
dbSNP Id: rs1131692204

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11111567G>T , CM000681.2:g.11111567G>T GRCh38
NC_000019.9:g.11222243G>T , CM000681.1:g.11222243G>T GRCh37
NC_000019.8:g.11083243G>T NCBI36
NG_009060.1:g.27187G>T , LRG_274:g.27187G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1372G>T ENSP00000252444.6:p.Glu458Ter
ENST00000559340.2:c.1114G>T ENSP00000453696.2:p.Glu372Ter
ENST00000560467.2:c.994G>T ENSP00000453513.2:p.Glu332Ter
ENST00000558518.6:c.1114G>T MANE Select ENSP00000454071.1:p.Glu372Ter
ENST00000252444.9:c.1368G>T
ENST00000455727.6:c.610G>T ENSP00000397829.2:p.Glu204Ter
ENST00000535915.5:c.991G>T ENSP00000440520.1:p.Glu331Ter
ENST00000545707.5:c.733G>T ENSP00000437639.1:p.Glu245Ter
ENST00000557933.5:c.1114G>T ENSP00000453557.1:p.Glu372Ter
ENST00000558013.5:c.1114G>T ENSP00000453346.1:p.Glu372Ter
ENST00000558518.5:c.1114G>T ENSP00000454071.1:p.Glu372Ter
ENST00000560173.1:n.113G>T
ENST00000560467.1:c.594G>T
NM_000527.4:c.1114G>T , LRG_274t1:c.1114G>T NP_000518.1:p.Glu372Ter
NM_001195798.1:c.1114G>T NP_001182727.1:p.Glu372Ter
NM_001195799.1:c.991G>T NP_001182728.1:p.Glu331Ter
NM_001195800.1:c.610G>T NP_001182729.1:p.Glu204Ter
NM_001195803.1:c.733G>T NP_001182732.1:p.Glu245Ter
XM_011528010.1:c.1114G>T XP_011526312.1:p.Glu372Ter
XM_011528011.1:c.733G>T XP_011526313.1:p.Glu245Ter
XR_244074.2:n.1264G>T
XM_011528010.2:c.1114G>T XP_011526312.1:p.Glu372Ter
XR_001753685.2:n.1231G>T
XR_001753686.2:n.1231G>T
NM_000527.5:c.1114G>T MANE Select NP_000518.1:p.Glu372Ter
NM_001195798.2:c.1114G>T NP_001182727.1:p.Glu372Ter
NM_001195799.2:c.991G>T NP_001182728.1:p.Glu331Ter
NM_001195800.2:c.610G>T NP_001182729.1:p.Glu204Ter
NM_001195803.2:c.733G>T NP_001182732.1:p.Glu245Ter